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1 male) were prospectively enrolled to undergo multipoint 4D flow magnetic resonance imaging.
2                 On these data we performed a multipoint affected sibling pair (ASP) linkage analysis
3  417 microsatellite markers were analyzed in multipoint allele sharing analyses.
4                  Analyses included a primary multipoint allele-sharing analysis (with ALLEGRO) and a
5 essive disorder, 88 SNPs were genotyped, and multipoint allele-sharing linkage analyses were carried
6                             The authors used multipoint allele-sharing methods to assess for linkage
7 for MI on chromosomal region 1p34-36, with a multipoint allele-sharing P value of <10(-12) (LOD=11.68
8                                              Multipoint analyses did not support the observation on c
9                                              Multipoint analyses were consistent with the two-point r
10                             Single-point and multipoint analyses were performed using various modific
11                                       In our multipoint analyses, measures of phonological memory dem
12 MHC region was supported by both 2-point and multipoint analyses, with the strongest peak (45.90 cM)
13                                              Multipoint analysis and haplotype reconstruction further
14                                              Multipoint analysis of 12 markers used for further fine
15 s demonstrated by either 2-point analysis or multipoint analysis of 17 microsatellites.
16                                              Multipoint analysis of abdominal skinfold with an LOD of
17                                              Multipoint analysis of affected relatives with CNV provi
18 e disequilibrium (LD) between markers during multipoint analysis of human pedigrees.
19                                Nonparametric multipoint analysis of left-handedness showed suggestive
20                                  Model-based multipoint analysis of the 10q25-q26 locus showed a loga
21 ficance for the different linkage tests, but multipoint analysis suggested a peak near D6S461.
22 1 for marker D1S3669 (34.2 cM), whereas with multipoint analysis the peak LOD was 2.58 at 35 cM.
23 lts confirm the accuracy of both programs in multipoint analysis with multiallelic markers on pedigre
24                                              Multipoint analysis yielded a maximum score of 5.94 at D
25                                              Multipoint analysis yielded a multipoint heterogeneity L
26 tional error checking (e.g., on the basis of multipoint analysis) be performed, beyond routine checki
27        Linkage in this area was supported by multipoint analysis, spanning 22.19 cM continuously from
28 location-specific African ancestry, based on multipoint analysis, was shifted upward in hypertensive
29 d by a 39.13-cM region (135.58-174.71 cM) in multipoint analysis, with the smallest P value (4.2 x 10
30 t all other polymorphisms are estimated by a multipoint analysis.
31 s identified on chromosome 6q by single- and multipoint analysis.
32 ken using MAPMAKER/SIBS for single-point and multipoint analysis.
33 sis and a maximum LOD score (MLS) of 4.44 in multipoint analysis.
34                  Using both single-locus and multipoint analytic methods, we found significant linkag
35 nomewide scans were conducted: single-point, multipoint, and multipoint performed on of white pedigre
36                                This point-to-multipoint architecture removes one of the main obstacle
37  the other signals across both two-point and multipoint, as well as parametric and nonparametric, ana
38  to improved power over existing methods for multipoint association mapping.
39 tionally weak affinity for cadherins through multipoint attachment to target cells, resulting in inhi
40 ctroscopy, scanning electron microscopy, and multipoint BET nitrogen adsorption/desorption.
41 ium (LE) between markers that underlies most multipoint calculation algorithms currently available, a
42 s of sharing alleles identical by descent in multipoint calculations and hence on type I error rates
43 ces capabilities for dynamic colorations and multipoint capacitive touch sensing.
44                             The slope of the multipoint cardiac index:central venous pressure relatio
45                                              Multipoint conditional analysis showed this effect to be
46                                          The multipoint contact analysis of the stereocontrolling tra
47 e RNA/mRNA duplex, is further facilitated by multipoint contacts across the RET2-specific middle doma
48                  Together, this work unveils multipoint contacts between PNKP and XRCC4-LigIV that re
49 tration that V2 neurons are sensitive to the multipoint correlations that are informative about natur
50  these computations--sensitivity to specific multipoint correlations--occur.
51  scenes or other complex signals with strong multipoint correlations.
52 ultipoint steady-state and continuous ramped-multipoint data acquisition methods.
53 scribe new statistical methods for analyzing multipoint data from admixture-mapping studies to detect
54 etermine reaction kinetics and argue how the multipoint detection gives useful insight into the molec
55 ion of PDFF with hepatic MR imaging by using multipoint Dixon techniques is highly reproducible acros
56                         A single-breath-hold multipoint Dixon-based acquisition was performed with co
57                   Data were analyzed using a multipoint engine for rapid likelihood inference and ord
58 t http://cansar.icr.ac.uk provides flexible, multipoint entry into canSAR.
59                                              Multipoint exclusion mapping rejected the hypothesis of
60                                              Multipoint FDAP analysis revealed that G-actin concentra
61  chromosome 13 findings were corroborated by multipoint findings, and extend our previous findings fr
62               Here, we use a newly developed multipoint fluorescence fluctuation spectroscopy techniq
63  LOD scores of 5.69 (single-point) and 4.52 (multipoint) for the pooled sample.
64 ugh variance component linkage analysis in a multipoint framework.
65                                            A multipoint fuel injection car (MPFI), direct-injection s
66                             Single-point and multipoint Haseman-Elston regression techniques were use
67 me genomic position also yielded the highest multipoint heterogeneity LOD (HLOD) score under a common
68 me genomic position also yielded the highest multipoint heterogeneity LOD (HLOD) score under a domina
69 ajor depression in males at marker D12S1300 (multipoint heterogeneity LOD score 4.6; P=.00003 after a
70 evidence became highly significant, with the multipoint heterogeneity LOD score at marker D12S1706 in
71 rametric linkage score of 1.57 and a maximal multipoint heterogeneity lod score of 2.11.
72                Multipoint analysis yielded a multipoint heterogeneity LOD score of 3.6 (alpha = 0.63)
73 t and multipoint LOD scores, as well as with multipoint heterogeneity LOD scores (HLODs) plus model-f
74 nce for linkage with both GD and HT (maximum multipoint heterogeneity LOD scores [HLOD] 2.0, 3.5, and
75  four or more affected individuals yielded a multipoint HLOD of 3.47 at 155 cM.
76  five or more affected individuals yielded a multipoint HLOD score of 4.26 at the same position.
77                               The parametric multipoint HLOD scores exceeded 3.0 for a 4-cM interval,
78  complementary supramolecular motifs, namely multipoint hydrogen bonding and metal complexation, as a
79  C-type inactivation gating is governed by a multipoint hydrogen-bond network formed by the triad Trp
80 thnic-specific marker allele frequencies and multipoint IBDs calculated in MERLIN.
81  LD exists can cause apparent oversharing of multipoint identity by descent (IBD) between sib pairs a
82                                              Multipoint interactions like the one presented herein ar
83        On the basis of marker information, a multipoint interval mapping method is provided to estima
84 al mouse parasite, Trichinella spiralis, and multipoint intravital time-lapse confocal microscopy of
85                                 Because full multipoint LD mapping can be slow, we exploited the hapl
86 ype-block structure at the analysis stage of multipoint LD mapping come from (1) greatly increased po
87                                  Model-free, multipoint linkage analyses (SIBPAL2, SAGE version 4.0)
88                                              Multipoint linkage analyses confirmed this interval and
89                                              Multipoint linkage analyses for insulin sensitivity phen
90                              Singlepoint and multipoint linkage analyses indicate that marker D10S165
91                       We therefore performed multipoint linkage analyses on both GFR measures using m
92                                Nonparametric multipoint linkage analyses were conducted, and the stro
93                                Two-point and multipoint linkage analyses were performed for all 218 f
94                      Genomewide, model-free, multipoint linkage analyses were performed separately fo
95                                              Multipoint linkage analyses were performed using data fr
96   Parametric and nonparametric two-point and multipoint linkage analyses were performed using the FAS
97                                Nonparametric multipoint linkage analyses were the primary approach, a
98                                              Multipoint linkage analyses were undertaken using both n
99                                              Multipoint linkage analyses were undertaken using both n
100 ults obtained from 46 U.S. families in which multipoint linkage analyses were undertaken using nonpar
101                                              Multipoint linkage analysis by GENEHUNTER2 gave the maxi
102                                              Multipoint linkage analysis identified quantitative trai
103 ncy estimation, parametric and nonparametric multipoint linkage analysis of discrete traits, variance
104                                     Combined multipoint linkage analysis of the VAGES and SAFDS data
105  a real-world dataset, performing parametric multipoint linkage analysis on a highly consanguineous p
106                                Two-point and multipoint linkage analysis revealed 2 distinct regions
107            Unfortunately, methods to perform multipoint linkage analysis scale poorly with either the
108                          These methods allow multipoint linkage analysis under oligogenic trait model
109                                Nonparametric multipoint linkage analysis was carried out using GeneHu
110  390 polymorphic markers were genotyped, and multipoint linkage analysis was conducted using the GENE
111                                              Multipoint linkage analysis was performed in all pedigre
112                                Two-point and multipoint linkage analysis was performed.
113 llelic markers as well as of full-chromosome multipoint linkage analysis with either diallelic or mul
114 oach resolves previously described biases in multipoint linkage analysis with SNPs that are in LD.
115                               Fine-structure multipoint linkage analysis yielded a maximum LOD score
116                                              Multipoint linkage analysis yielded the strongest eviden
117                                              Multipoint linkage analysis yielded the strongest eviden
118                                              Multipoint linkage analysis, under a simple autosomal do
119                       Using single-point and multipoint linkage analysis, we detected a modest but si
120 nce is an important and difficult problem in multipoint linkage analysis.
121 p will enable empiric coverage estimates and multipoint linkage analysis.
122 nce-components technique was used to conduct multipoint linkage analysis.
123                                              Multipoint linkage and haplotype analysis narrowed the l
124 nd single-nucleotide polymorphisms and a new multipoint linkage disequilibrium method that searches f
125 ores for 2 markers near the centromere, with multipoint linkage indicating a CSS trait locus spanning
126                              In their study, multipoint linkage methods were applied to affected sib-
127 falling under the second highest genome-wide multipoint linkage peak, multipoint logarithm of odds, 1
128                                         Most multipoint linkage programs assume linkage equilibrium a
129            Graphical outputs of whole genome multipoint linkage statistics are provided allowing comp
130 ge analysis, and computed both two-point and multipoint linkage statistics.
131 inkage analysis was performed with MLINK and multipoint linkage with SimWalk 2.89.
132 by developing novel methods for case-control multipoint linkage-disequilibrium (LD) mapping that gain
133 een suggested that traditional nonparametric multipoint-linkage procedures can show a "bias" toward t
134                                          The multipoint locus homogeneity LOD in the 35 pedigrees was
135 omosome 1 at approximately 218 cM from pter (multipoint LOD 1.80) and on chromosome 10 at approximate
136 omosome 10 at approximately 86 cM from pter (multipoint LOD 2.07); to current fasting glucose levels
137 omosome 10 at approximately 96 cM from pter (multipoint LOD 2.15); and to HbA(1c) levels on chromosom
138 e of linkage and association with 8q12 loci (multipoint LOD 2.77; P=.0028).
139 els on chromosome 1 at approximately 187 cM (multipoint LOD 2.81).
140 OD = 3.3; empirical P value <.001) and 5q31 (multipoint LOD = 1.4; empirical P value <.081) met these
141                 Regions on chromosomes 3q13 (multipoint LOD = 3.3; empirical P value <.001) and 5q31
142  haplotype configuration (in addition to the multipoint LOD graph for linked pedigrees) was used to i
143 a paternal effect (single-point LOD of 4.79; multipoint LOD of 3.72 for BMI) in region 13q32, in the
144 a maternal effect (single-point LOD of 2.85; multipoint LOD of 4.01 for body mass index [BMI] and 3.6
145 ly one other region in the genome produced a multipoint LOD score >1 (LOD = 1.3).
146 me 6p21) was evident, exhibiting the highest multipoint LOD score (4.96 at marker HLA-B).
147 i.e. two-point lod score (TLS) >/=1.9 and/or multipoint lod score (MLS) >/=2.2] in at least one of ou
148 ilies, LRRK2 G2019S segregates with disease (multipoint LOD score 2.41).
149 omozygous locus (D19S565 to D19S884, maximum multipoint LOD score 3.28) on chromosome 19p13 to which
150 CA) IMT (two-point log odds [LOD] score 4.1, multipoint LOD score 3.4) was found 161 cM from the tip
151 were confirmed using the GENEHUNTER package (multipoint LOD score 4.3).
152  compatible with linkage to chromosome 4q21 (multipoint LOD score 5.5).
153                                              Multipoint lod score and nonparametric (Zlr score) linka
154                                     The peak multipoint LOD score is located 1 cM away from the uridi
155 3.1 cM from the 11p telomere, with a maximum multipoint LOD score of 1.8.
156  of which chromosome 5p13.1 gave the highest multipoint lod score of 2.7.
157 h microsatellite markers generated a maximal multipoint LOD score of 3.02 (theta = 0) at D9S1878.
158 n two families (two-point LOD score of 3.77; multipoint LOD score of 3.91).
159 s with additional families yielded a maximum multipoint LOD score of 3.93 on chromosome 18, a two-poi
160                                  The maximum multipoint LOD score of 4.10 was obtained for 4 markers:
161  the authors found a genome-wide significant multipoint LOD score of 4.14 for major depressive disord
162 maximum single-point LOD score of 4.33 and a multipoint LOD score of 4.75 were found in a 15-20 cM re
163                    We previously published a multipoint LOD score of 4.9 at D7S1804 for BMI from the
164                                    A maximal multipoint LOD score of 4.9 was obtained between D6S286
165 e additional markers, resulting in a maximum multipoint LOD score of 5.0 for FEV1 at 184.5 cM.
166 al on chromosome 12p13, generating a maximum multipoint LOD score of 5.17.
167 n on chromosome 19p13.3-p13.2 with a maximum multipoint LOD score of 5.338 at markers D9S427 and D9S1
168 ers (total 28 members) that showed a maximum multipoint LOD score of 5.4 in the 9q31-q32 region, unde
169 is family on chromosome 11q25 with a maximum multipoint LOD score of 6.15.
170 wo-point LOD score was 3.98, and the maximal multipoint LOD score was 4.57.
171 ly significant increase in the nonparametric multipoint LOD score was observed on chromosome 2q34, wi
172 p12-p13.2 between markers D2S292 and D2S289 (multipoint LOD score Z(max) = 3.01 at D2S145).
173 e disease to chromosome 17p12-p13.1 (maximum multipoint lod score, 4.39).
174 LOD scores >1.5, together with nonparametric multipoint LOD scores >1.0.
175                                              Multipoint LOD scores for saturated fat dropped to 1.27
176                                  The maximum multipoint LOD scores for the heritable quantitative bio
177 egions yielded nonsignificant but suggestive multipoint lod scores greater than 2.5, with the stronge
178             Fourteen of the 19 loci that had multipoint LOD scores of >1.5 were near to or overlapped
179 us to canine chromosome 8 with two-point and multipoint lod scores of 10.8 and 14, respectively.
180 vely linked to regions on chromosome 18 with multipoint LOD scores of 2.4 for FEV1 and 1.5 for FVC at
181 arker and CL/P was assessed by two-point and multipoint LOD scores, as well as with multipoint hetero
182 rkers used simultaneously for computation of multipoint LOD scores.
183 2 affected members of this family revealed a multipoint LOD(max) of 3.27 on chromosome 12q.
184 ta from 13 members of this family revealed a multipoint LOD(max) of 3.31 on chromosome 5q31.
185  responsiveness was identified at chr8p21.3 (multipoint LOD=4.11; teacher/parent scores) and chr8q24.
186 4.11; teacher/parent scores) and chr8q24.22 (multipoint LOD=4.54; parent-only scores), respectively.
187 s confirmed significant linkage; the largest multipoint log odds ratio score was 5.6 at D12S351.
188 oint score 3.281 (P = 0.0005) and parametric multipoint log of the odds (LOD) score 2.983.
189 p13, and linkage analysis yielded a combined multipoint log(10) odds (LOD) score of 3.6.
190  identified on chromosome 4q, with a maximum multipoint logarithm of odds (LOD) score (MLS) of 3.1 in
191 1.5 cM from the 11p telomere, with a maximum multipoint logarithm of odds (LOD) score of 2.4.
192 titative traits and to calculate 2-point and multipoint logarithm of odds (LOD) scores using a polyge
193 approximately 247 cM from p-telomere (pter) (multipoint logarithm of odds [LOD] 2.33) and on chromoso
194 ne on chromosome 10p12.1-p13 was identified (multipoint logarithm of odds score 3.25).
195 bility locus to chromosome 2q with a maximum multipoint logarithm of odds score of 1.6 in 378 affecte
196                                  The highest multipoint logarithm of odds score of 3.3 was found at 1
197  the long arm of human chromosome 21, with a multipoint logarithm of odds score of 3.9 noted near mar
198 bismus susceptibility locus to 7p22.1 with a multipoint logarithm of odds score of 4.51 under a model
199 idate region on chromosome 17 with a maximum multipoint logarithm of odds score of 6.01.
200 In black individuals, the univariate maximum multipoint logarithm of odds scores (MLS) were observed
201  a maximum "location score" (comparable with multipoint logarithm of odds scores) of 3.191.
202 highest genome-wide multipoint linkage peak, multipoint logarithm of odds, 1.59.
203 nalysis and fine mapping generated a maximum multipoint logarithm of the odds (LOD) score of 3.0 at c
204 w locus for distal myopathy at 9p21.2-p22.3 (multipoint logarithm of the odds ratio=4.21).
205  to a 25-cM region on 3p24-25 with a maximum multipoint logarithm of the odds score of 4.28.
206 ion, and this was confirmed using a Bayesian multipoint mapping analysis.
207                          By using a Bayesian multipoint mapping method and visual inspection of signi
208 k information to develop a fast single-block multipoint mapping method.
209 PL-log [P value] >12 at approximately 12 cM; multipoint maximum location score 2.48 [alpha = 0.10] at
210                                              Multipoint maximum LOD score (MLS) analysis yielded sign
211                                              Multipoint maximum LOD scores (MLS) obtained from affect
212  factor, improving the applicability to most multipoint measurements that would traditionally be achi
213                  Here we define a model-free multipoint method on the basis of dense sequence polymor
214               Liang et al. proposed a robust multipoint method that can be used to simultaneously est
215 her single-point estimates or rather complex multipoint methods of inferring individual autozygosity,
216  in this area is the development of powerful multipoint methods that can detect causal variants that
217                                            A multipoint model is proposed, based on well-established
218 en sib pairs and false-positive evidence for multipoint model-free linkage analysis of affected sib p
219                                              Multipoint, model-free ARP linkage analysis was performe
220 we developed and implemented time-integrated multipoint moment analysis (TIMMA), a form of fluorescen
221                                              Multipoint monitoring of a subject in an advanced drivin
222 For venous blood flow, the ICC with Bayesian multipoint MR imaging was significantly larger than that
223      These findings indicate that the use of multipoint NIR spectroscopy can achieve representative q
224                  The present study evaluated multipoint NIR spectroscopy for in-line moisture content
225 n a freeze-dryer shelf was possible with the multipoint NIR system in use.
226                                              Multipoint non-parametric linkage analyses were performe
227 ype D11S4124-D11S2349-D11S1338-D11S1323, and multipoint nonparametric analysis (NPL) confirms this fi
228                                Two-point and multipoint nonparametric linkage (NPL) analyses were con
229 m multipoint parametric LOD score of 4.1 and multipoint nonparametric linkage (NPL) LOD score of 3.2.
230 ptibility locus on chromosome 9p24-22 with a multipoint nonparametric linkage (NPL) score of 3.22.
231 ng LOD score from LODPAL = 5.77 at D11S1998; multipoint nonparametric linkage [NPL]-log[P value] = 5.
232                                Two-point and multipoint nonparametric linkage analyses were performed
233                      Linkage was assessed by multipoint nonparametric linkage analyses.
234 tained 296 ESRD-affected sibling pairs using multipoint nonparametric linkage analysis methods.
235                                              Multipoint nonparametric linkage analysis revealed evide
236                                              Multipoint nonparametric linkage analysis revealed highl
237 386 microsatellite markers were subjected to multipoint nonparametric linkage analysis.
238 e analysis with the two SNPs, with a maximal multipoint nonparametric linkage score of 1.57 and a max
239                                     Here, by multipoint nonparametric linkage, pedigree structure all
240                                              Multipoint, nonparametric linkage analyses were conducte
241 cgammaRIIA (single-point NPL 2.0, P = 0.021; multipoint NPL 2.6, P = 0.006) loci, but not the Fcgamma
242  nonparametric linkage [NPL] 1.8, P = 0.038; multipoint NPL 2.7, P = 0.004) and the FcgammaRIIA (sing
243 ears of age (n = 39 families) gave a maximum multipoint NPL score of 2.65 (P = 0.007).
244 -free identity-by-descent statistics and the multipoint NPL statistic.
245  = 5.49 at approximately 128 cM), and 17p11 (multipoint NPL-log [P value] >12 at approximately 12 cM;
246 availability of high-density genome scans, a multipoint, observational method of estimating individua
247 ro gas chromatography (microGC) detector for multipoint on-column detection.
248 trate the effectiveness of this approach for multipoint optical stimulation in the mammalian brain in
249 marker in the leptin gene on 7q31 (empirical multipoint P = 0.0004) in whites.
250 line fasting glucose on 12q13-q14 (empirical multipoint P = 0.0006).
251 ome 10p is potentially linked to DN (CA only multipoint P = 4 x 10(-3)).
252 in the Beaver Dam Eye Study sample (D15S659, multipoint P=.047), but is otherwise novel.
253 f a major locus on chromosome 15q (GATA50C03 multipoint P=1.98x10-7; empirical P< or =1.0x10-5; singl
254                                              Multipoint PAP-flow relationships are usually described
255                                              Multipoint parametric analysis gave a logarithm of odds
256                                              Multipoint parametric analysis performed by use of GENEH
257                     Two-point parametric and multipoint parametric and nonparametric analyses were pe
258                                    A maximum multipoint parametric heterogeneity LOD (HLOD) score of
259                               We performed a multipoint parametric linkage analysis on a cohort of F(
260                                              Multipoint parametric linkage analysis revealed identica
261                                              Multipoint parametric linkage analysis with 13 members o
262                                              Multipoint parametric LOD score calculation in this fami
263            One KTCN family yielded a maximum multipoint parametric LOD score of 4.1 and multipoint no
264 he long arm of chromosome 5 with a combined, multipoint parametric LOD score of 6.21.
265                    We obtained a significant multipoint parametric logarithm of odds score of 3.3 on
266 hidden Markov model, our approach allows for multipoint pedigree analysis with large numbers of SNP m
267 ere conducted: single-point, multipoint, and multipoint performed on of white pedigrees only (92% of
268                                            A multipoint posterior probability of linkage analysis of
269 riance-components methods), genetic linkage (multipoint quantitative trait analyses), and association
270           The following regions had positive multipoint results (HLOD > or =1.0 and/or NPL P< or =.05
271 e investigated in the setting of genome-wide multipoint scans.
272 p23 with maximal nonparametric linkage (NPL) multipoint score 3.281 (P = 0.0005) and parametric multi
273 gns, to an interval of consecutive probes, a multipoint score that parsimoniously captures the underl
274 POE) genotypes were used as a covariate in a multipoint sibpair analysis.
275 21, 16p12, 18p11, and 20q13), with a nominal multipoint significance level of P< or =.01 or LOD > or
276                                              Multipoint single-locus linkage analysis provided modest
277 istical algorithm to map TSGs, using a novel multipoint statistical score function.
278                   Traditional nonparametric "multipoint" statistical procedures have been developed f
279 is technique can be extended to the discrete multipoint steady-state and continuous ramped-multipoint
280                                   The 1-HLOD multipoint support interval from the multigenerational f
281 s with the deletion allele and are obtaining multipoint survival-vs.-dose assays in at least one homo
282                            We apply a unique multipoint time correlation function analysis to the mic
283 Using an immunoaffinity approach followed by multipoint validation, we identified the target of serin
284                                 We performed multipoint variance component linkage analysis in each c
285                                              Multipoint variance component linkage analysis was perfo
286                                              Multipoint variance component-based linkage analysis was
287                                              Multipoint variance components linkage analyses revealed
288                                              Multipoint variance components linkage analysis (GENEHUN
289                                              Multipoint variance components linkage analysis using a
290                                              Multipoint variance components linkage analysis was perf
291 -wide linkage scans were carried out using a multipoint variance components method in white and black
292                                              Multipoint variance-component linkage analysis was perfo
293                                              Multipoint variance-component linkage analysis was perfo
294 ccurrence and a 10-cM gene map, we performed multipoint variance-components analysis to localize susc
295 r Genetics Initiative was performed by using multipoint variance-components linkage analysis.
296                                     Bayesian multipoint velocity-encoded MR imaging allows for simult
297 n arterial blood flow measured with Bayesian multipoint velocity-encoded MR imaging and that measured
298 ence between CSF flow measured with Bayesian multipoint velocity-encoded MR imaging and that measured
299 n, five women) by using accelerated Bayesian multipoint velocity-encoded MR imaging.
300 scribe pin-hole array correlation imaging, a multipoint version of fluorescence correlation spectrosc

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