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1 ns close to IFNG (chromosome 3) and the MHC (chromosome 20).
2 pped to overlapping loci on the short arm of chromosome 20.
3 ther failed or had shown no abnormalities of chromosome 20.
4 lls was attributable to additional copies of chromosome 20.
5 ransglutaminase-2 and transglutaminase-3, on chromosome 20.
6 ated loci, with the strongest association on chromosome 20.
7  ZBTB46 gene was driving the association for chromosome 20.
8 g defined a 26-Mb candidate region in canine chromosome 20.
9 terspecific F(2) population, now known to be chromosome 20.
10 f 3 S100A genes on chromosome 1 and SLPI1 on chromosome 20.
11 o a region of increased number of alleles on chromosome 20.
12  genes that now map to the long arm of human chromosome 20.
13 9 highly polymorphic loci on the long arm of chromosome 20.
14 tion is conserved at the human NNAT locus on chromosome 20.
15 ll line (passage 10) as well as a trisomy of chromosome 20.
16  critical region and spaced over the rest of chromosome 20.
17 ween type 2 diabetes and any other region on chromosome 20.
18  disorders characterized by abnormalities of chromosome 20.
19 t least two diabetes-susceptibility genes on chromosome 20.
20 ybrid panel, neuronatin gene was assigned to chromosome-20.
21 r changes were identified, including gain of chromosomes 20, 13, and 8q and smaller regions of amplif
22 egion of linkage has thus been identified on chromosome 20 (20p12).
23 rmed Parkinson's disease on the short arm of chromosome 20 (20pter-p12) and identify TMEM230 as the d
24 f DNA sequences derived from the long arm of chromosome 20 (20q) has been commonly observed by both c
25 kage region for OA of the first CMC joint on chromosome 20 (4 cM; LOD score 3.74).
26 omosome 7 (16.8%), chromosome 5 (10.9%), and chromosome 20 (9.9%) were observed among low-grade epile
27 CEPH) pedigree data across a 10-Mb region of chromosome 20, a comparison of population recombination
28 al specimens by obtaining new information on chromosome 20 aberrations in breast cancer.
29 crosis/fibrosis after treatment, and gain of chromosome 20, all indicators of resistance to chemother
30 gion on the Y was identified covering 80% of Chromosome 20, allowing some first inferences on the rec
31 rit susceptibility genes simultaneously from chromosome 20 and chromosome 12.
32 lved in cardiac development-MYH7B/miR499A on chromosome 20 and CTSK, CTSS and ARNT on chromosome 1.
33  the recently discovered BBS6 gene (MKKS) on chromosome 20 and for potential assignment of the disord
34 tive neoplasms (MPN) affects the long arm of chromosome 20 and has been predicted to harbor a tumor s
35 haly and periventricular heterotopia maps to chromosome 20 and is caused by mutations in the gene ADP
36 h kindred, we identified a linkage region on chromosome 20 and selected candidate genes for screening
37 detected by Southern blot hybridization from chromosome 20 and, indeed, from the remainder of the gen
38            And, using deletion constructs of chromosome-20 and fluorescence in situ hybridization, ne
39 ON 1), the strongest linkage results were on chromosomes 20 and 11.
40 phic loci that map to the long arms of human chromosomes 20 and 12 in regions containing the MODY1 an
41 replicate single-nucleotide polymorphisms on chromosome 20 (and putatively on the THBD gene for throm
42 in 2,020 CpG islands on human chromosome 12, chromosome 20, and 34 selected regions.
43  angle glaucoma (POAG) to a 4-Mb interval on chromosome 20, and identified a Gly661Arg variant in ADA
44  2, a region of syntenic homology with human chromosome 20, and in a region containing a number of ge
45 genes have been previously mapped to buffalo chromosome 20, and sequence detail is limited, so 65 mar
46 econd family member is predicted to exist on chromosome 20 approximately 4 kb downstream from Eppin's
47 ther genes (SNAI1 and KRML) mapping to human chromosome 20 are also duplicated in Fugu.
48                  We demonstrate that SNPs on chromosome 20 are cis-eQTLs for thrombomodulin (THBD), a
49 amplification of 1q21.3 (including HRNR) and chromosome 20 are shared by SC-O and SC-E, as is deletio
50 t type 2 diabetes located on the long arm of chromosome 20 around marker D20S196.
51 llites, identified a region of near 13 cM in chromosome 20 as the best candidate to harbour the causa
52 osomes were identified for CKIIalpha: one on chromosome 20 band 13 with an approximate size of 20 kb
53 n KRML gene within a genomic contig on human chromosome 20, bands q11.2-q13.1.
54                The human gene (POFUT1) is on chromosome 20 between PLAGL2 and KIF3B, near the centrom
55 and 14 restriction site polymorphisms) and Y-chromosome (20 biallelic polymorphisms and 5 short tande
56  new maps of river buffalo (Bubalus bubalis) chromosome 20 by both dissociation curve analysis and co
57  been localized to a 9-centimorgan region of chromosome 20 by homozygosity mapping.
58               The finished sequence of human chromosome 20 comprises 59,187,298 base pairs (bp) and r
59 es) in the "MODY1 region" of the long arm of chromosome 20 contributes to the development of NIDDM, w
60  iLASH, RaPID, and TRUFFLE) using UK Biobank chromosome 20 data and simulated sequence data.
61 ome data set of 30 million reads and a human Chromosome 20 data set of 1.7 million reads.
62                A deletion of the long arm of chromosome 20, del(20q), is a recurring abnormality in m
63 mut) patients had an increased prevalence of chromosome 20 deletions and ASXL1 mutations.
64 ative trait loci (QTL) cqSeed protein-003 on chromosome 20 exerts the greatest additive effect of any
65 didymal protease inhibitor), a gene on human chromosome 20 expressing three mRNAs encoding two isofor
66 syntenic relationships between LG8 and human chromosome 20, extended existing synteny between LG7 and
67 ed their disease gene to a 21.6-cM region of chromosome 20 flanked by markers D20S888 and D20S102.
68 as cloned during a search on the long arm of chromosome 20 for genes whose expression and copy number
69    The human L3MBTL gene lies in a region of chromosome 20 frequently deleted in patients with myeloi
70                 Deletions of the long arm of chromosome 20 have been reported in a wide range of myel
71                  Linkage to the short arm of chromosome 20 in a genome screen was followed by positiv
72 igh-coverage whole genome sequencing data of chromosome 20 in about a third of the space of its BCF f
73             The human OTOR gene localizes to chromosome 20 in bands p11.23-p12.1 and more precisely t
74                   The characteristic loss of chromosome 20 in BIA-ALCL provides further justification
75 ation rates ( rho ) along a 10-Mb stretch of chromosome 20 in four population samples, comprising Eas
76  revealed 1 overlapping homozygous region on chromosome 20 in the consanguineous families.
77 dentified a genome-wide association locus on chromosome 20 in the discovery cohort; functional annota
78 e-restricted imprinting of a gene cluster on chromosome 20 in the region commonly deleted in chronic
79 fied a major susceptibility factor, Cia1, on chromosome 20 in the vicinity of the rat major histocomp
80 We observed a switch error rate of 0.0016 on chromosome 20 in the White British trio offspring.
81 mmon markers across a 10 Mb segment of human chromosome 20 in three samples (UK Caucasian, CEPH Cauca
82 ition on chromosome 2 at 8.5 cM, the MLS for chromosome 20 increases to 5.50 at 69.0 cM (P=.0014).
83  element on chromosome 7 and possibly one on chromosome 20 influence susceptibility to diabetic nephr
84                    Nonparametric analysis of chromosome 20 inheritance data collected with the MODY1-
85      An acquired deletion of the long arm of chromosome 20 is a recurrent abnormality in myeloprolife
86  erythematosus (SLE) susceptibility genes on chromosome 20 is suggested by the observation of genetic
87 tion of coding DNA without high entropy, and chromosome 20 is the opposite with a low frequency of co
88 ignificantly improved the LOD scores at both chromosome 20 locations (20p12 LOD = 5.06 and 20q13 LOD
89  score for log(TG/HDL-C) = 1.1 at 75 cM] and chromosome 20 [LOD score for log(TG/HDL-C) = 1.7 at 35 c
90 ucokinase gene markers GCK1 and GCK2 and the chromosome 20 marker D20S197.
91 uble minute chromosomes (DMs) that contained chromosome 20 material in cell lines with 20q13.2 amplif
92 LOD] = 2.08), chromosome 9q (MaxLOD = 2.00), chromosome 20 (MaxLOD = 1.82), and chromosome 21 (MaxLOD
93  the genes that are mutated in MODY on human chromosomes 20 (MODY1), 7 (MODY2) and 12 (MODY3), with M
94 nal, with a Z score of 2.05, was observed on chromosome 20 near marker D20S195, and another on 20p ne
95 2) and D9S302 (two-point LOD = 1.28); and on chromosome 20, near D20S115 (multipoint LOD = 1.83) and
96                              FISH with whole chromosome 20 paint showed expanded chromosome regions (
97 e l3mbtl1 gene is located on the long arm of chromosome 20 (q12), within a region commonly deleted in
98                  Deletion of the long arm of chromosome 20 represents the most common chromosomal abn
99             Genotyping of additional STRs on chromosome 20 resulted in improved evidence for linkage
100 eplicated single-nucleotide polymorphisms on chromosome 20 (rs2144940, rs2567617, and rs1998081) that
101 , we identified a new melanoma risk locus on chromosome 20 (rs910873 and rs1885120), with replication
102 .012 false positive rate simultaneously on a chromosome 20 sequencing panel having 86 265 sites.
103                                              Chromosome 20 showed our strongest initial evidence for
104 region syntenic with a large region of human chromosome 20, showing linkage to percent body fat (like
105 jacent genes found within a 300 kb region of chromosome 20, suggesting that they may be under transcr
106 20q shares synteny conservation with chicken chromosome 20, suggesting the segment to be ancestral in
107 tic variants linked to kidney dysfunction on chromosome 20 target the acyl-CoA synthetase short-chain
108 ymorphic markers across a 98.5-cM segment of chromosome 20 that contains the candidate region.
109                   One signal was for CD93 on chromosome 20; this gene is not strongly expressed in th
110      Comparative analysis of the sequence of chromosome 20 to whole-genome shotgun-sequence data of t
111 dromes in whom a deletion of the long arm of chromosome 20 was detectable by G-banding and/or fluores
112 y found the genetic polymorphism of PCSK2 on chromosome 20 was responsible for the linkage peak of se
113                               While studying chromosome 20, we found a locus on chromosome 20q11.2 th
114             Trisomies of chromosome 7 and/or chromosome 20 were detected in 17 of 20 colorectal tumor
115 ders, three significant associations, all on chromosome 20, were identified: rs4809706 (p-value: 2.8
116 ing exon and an extension of the analysis to chromosome 20, where the MMP-9 gene is located, suggesti
117                Our strongest results are for chromosome 20, where we observe a weighted maximum LOD s
118 it loci (QTLs) in common, i.e., Aia1/Cia1 on chromosome 20, which includes the MHC, and Aia3/Cia3 on
119  LD using 43 microsatellite markers spanning chromosome 20 with an average density of 2.3 cM.
120 To date, our best evidence for linkage is on chromosome 20 with potentially separable peaks located o

 
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