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1 oncarriers to establish clinical and genetic cosegregation.
2       For 2 novel TNNI3K variants, we tested cosegregation.
3 y is not possible without data demonstrating cosegregation.
4 mmetric self-renewal and immortal DNA strand cosegregation.
5 mmetric self-renewal and immortal DNA strand cosegregation.
6 mily members to establish genotype-phenotype cosegregation.
7 ly coupled by physical linkage and resulting cosegregation.
8 tentially disease-causing gene variants with cosegregation, a novel hyperpolarization-activated cycli
9                         Limited phylogenetic cosegregation among hepatoviruses and their hosts and re
10 ygosity mapping, whole-exome sequencing, and cosegregation analyses were used to identify gene varian
11 lysis and confirmed by Sanger sequencing and cosegregation analyses.
12 Identification of a second mutant allele and cosegregation analysis confirmed correlation with the mu
13                                              Cosegregation analysis in each available family showed t
14  genes and to evaluate disease penetrance by cosegregation analysis in family members.
15  569 FPF kindreds was performed, followed by cosegregation analysis in large kindreds, gene burden an
16 t genomic sequencing and, where possible, by cosegregation analysis in the families of the index case
17 fied >500 seedling-lethal mutants, completed cosegregation analysis of the insertion and the lethal p
18                                              Cosegregation analysis of TIMP3 variants was performed i
19                                              Cosegregation analysis revealed 5.5- and 2.4-kb Mu1-hybr
20 ed in an active Mutator (Mu) population, and cosegregation analysis revealed that it arose from a Mu3
21                                              Cosegregation analysis showed that the functional y1 gen
22 nts were confirmed by Sanger sequencing, and cosegregation analysis was performed in families, follow
23           Random marker genome screening and cosegregation analysis were performed on F2 hybrids deri
24 The authors were unable to determine through cosegregation analysis whether three other changes encou
25  quantitative polymerase chain reaction, and cosegregation analysis.
26 ix additional affected family members showed cosegregation and a maximum LOD score of 3.6.
27  as HCM-linked or nonpathogenic according to cosegregation and population genetics criteria.
28                              Our sequencing, cosegregation and rescue results indicate that suc encod
29 MP guidelines is the lack of a definition of cosegregation as criteria for pathogenicity classificati
30  causal for a phenotype based on the variant cosegregation as well as a priori evidence such as delet
31                                      Further cosegregation, complementation, and comparative analyses
32 n small families and sporadic cases, wherein cosegregation could not be established.
33                                              Cosegregation data differ from many other types of patho
34  evolution, including frequent PB2-PB1-PA-NP cosegregation during avian influenza reassortment.
35 how intersegment RNA interactions drive vRNP cosegregation during reassortment between different IAV
36 t of LD, suggesting the need to model LD and cosegregation explicitly.
37 nscriptome analysis, gene expression assays, cosegregation in F(2) plants and functional tests to ide
38 nscriptome analysis, gene expression assays, cosegregation in F(2) plants and functional tests to ide
39        We evaluated deleterious variants for cosegregation in families and assessed clinical characte
40 own inconsistent results; there is a lack of cosegregation in some pedigrees and an unexpectedly high
41         Sanger sequencing confirmed complete cosegregation in the family.
42  MODY-associated variants showed only modest cosegregation in these genes.
43                                              Cosegregation information also declines with increasing
44                   We provide machine-learned cosegregation information for over 700 ternary aluminum-
45                                              Cosegregation information from half sibs contributes lit
46 ese analyses reveal that immortal DNA strand cosegregation is also regulated by IMPDH and confirm the
47 idate the concept in one ternary alloy where cosegregation is not expected by prior models but is exp
48 al implicit precept that immortal DNA strand cosegregation is specific to cells undergoing asymmetric
49 its confounded effect on the pattern of gene cosegregation, it complicates linkage analysis and map c
50                     For tightly linked loci, cosegregation may lead to nonrandom associations between
51                                     However, cosegregation of a mutant allele with the disease phenot
52 erged that suggested at least some degree of cosegregation of ADHD and learning disabilities in famil
53 sk for DESR and cannot determine whether the cosegregation of ADHD in DESR within families is a resul
54 he existence of immortal DNA strands and the cosegregation of chromosomes that bear them.
55 ed a second, ethnically distinct, family for cosegregation of disease with markers from the linked re
56                                              Cosegregation of epilepsy and deafness was not observed
57                            Reports proposing cosegregation of genes found on the X chromosome with bi
58 on suppression over large genomic tracts and cosegregation of genes of various functions, not necessa
59 latedness, and attempts are made to identify cosegregation of genetic markers and phenotypes within t
60 ons-sex concordance in sib pairs with HD and cosegregation of HD and LWD-impelled a test of the hypot
61 n bipolar affective disorder (BPAD) revealed cosegregation of high numbers of EvC and Bipolar I (BPI)
62 bsequent lineage restrictions, an unexpected cosegregation of lymphoid and myeloid gene expression an
63                                              Cosegregation of MNGIE with a single chromosomal region
64  In each of these families there is complete cosegregation of mood disorder with a segment of chromos
65             Particularly in small pedigrees, cosegregation of multiple mutations, occasional unawaren
66              These results were supported by cosegregation of MYOCD variants with the phenotype in 4
67 this phenomenon occurs involves preferential cosegregation of nonparental chromatids of both chromoso
68 eviously linked to schizophrenia through the cosegregation of oculocutaneous albinism with psychosis
69                                We report the cosegregation of point mutations in the neuroserpin gene
70                                              Cosegregation of profound, congenital deafness with mark
71                 This is unfortunate, because cosegregation of rare variation and disease status in fa
72                           There was a strong cosegregation of SFB positivity and diabetes protection
73                                              Cosegregation of single-nucleotide polymorphism-defined
74 regation, since deletion of clp1/flp1 causes cosegregation of sister chromatids, when sister kinetoch
75                                              Cosegregation of template DNA during mitosis is one mech
76 1ADE2 inserted into a YAC were identified by cosegregation of the ADE2 gene with the URA3-marked YAC.
77 inkage analysis of F2(SxR) male rats detects cosegregation of the alpha1 Na,K-ATPase locus with salt-
78 n F2 and two backcross populations indicated cosegregation of the augmented orf107 and urf209 process
79              The results clearly demonstrate cosegregation of the branch-point mutation with the CCA
80  did the seeds of the F1 hybrids, indicating cosegregation of the genes for rosette size and the germ
81     Studies of human-mouse chimeras revealed cosegregation of the high (36)Cl(-) transport phenotype
82 forbold locus-specific haplotyping to detect cosegregation of the locus haplotype with the phenotype,
83                                     Complete cosegregation of the mutation with reduced free protein
84 milial PA, whole-exome sequencing identified cosegregation of the PA phenotype with the heterozygous
85                                           By cosegregation of the phenotype with a satellite marker a
86                                              Cosegregation of the repeat expansion with disease in th
87 integrated into the nuclear genome, (2) show cosegregation of the resistance phenotype with the intro
88                                          The cosegregation of the traits is attributed to tight linka
89 s can be combined with data from analysis of cosegregation of the UCVs with cancer, co-occurrence of
90 D is prevented by missing data demonstrating cosegregation of the variants and incomplete knowledge a
91                             In addition, the cosegregation of these phenotypes allows us to postulate
92                      The significance of the cosegregation of this phenotype and B-1a cell expansion
93                                              Cosegregation of this region with disease in different e
94 associated genes and the ability to test for cosegregation of variants with disease through extended
95 ression analysis reveals enrichment, but not cosegregation, of clinical and genetic disease features
96  of a pedigree, even if they have reasonable cosegregation patterns.
97                                              Cosegregations resulting in significant increases of T2D
98                                              Cosegregation studies could not be performed on the pati
99  limits their number and immortal DNA strand cosegregation that limits their accumulation of mutation
100 and additive-genetic relationships, but also cosegregation to capture relationships at QTL.
101 bers were genotyped by Sanger sequencing and cosegregation was analyzed.
102 hment of TBX20tv in DCM/LVNC was calculated, cosegregation was determined in selected families, and c
103                                 Template DNA cosegregation was enhanced by cell-cell contact.
104                                      Perfect cosegregation was observed for broccoli and cauliflower
105                         Moreover, oligogenic cosegregation was suggestive for complex inheritance and
106            Testing of the CMM abundances for cosegregation with 530 fully informative SNP markers ide
107 s and emphasizes the importance of observing cosegregation with deafness in large families to confirm
108 variants in BLK, KLF11, and PAX4 showed poor cosegregation with diabetes (combined logarithm of the o
109  We examined variant-level genetic evidence (cosegregation with diabetes and frequency in population)
110 subjects, and no evidence for association or cosegregation with disease in family-based analyses.
111 and, in a subset of probands, an analysis of cosegregation with disease in pedigrees.
112 ino acid position in multiple pedigrees, and cosegregation with disease in these pedigrees provide ev
113 g studies because they provide a way to test cosegregation with disease of variants that are too rare
114                                          The cosegregation with hypertension of an impaired D1 recept
115 ling endosomes, show preferential asymmetric cosegregation with lysosomes.
116                  All analyses excluded CYP19 cosegregation with PCOS, demonstrating that this locus i
117         Mutations were examined for familial cosegregation with phenotype and presence or absence in
118                                              Cosegregation with phenotype was confirmed in additional
119 cluded from the EDA locus by the lack of its cosegregation with polymorphic markers flanking the EDA
120 ers of 188 HPC families and tested for their cosegregation with prostate cancer.
121 ns, were initially identified based on their cosegregation with S alleles.
122 ulum-anchored lipid transfer protein, showed cosegregation with syndromic ID in both families.
123 tation can be observed in many relatives and cosegregation with TG can be tested.
124                          Nevertheless, given cosegregation with the 6p25.3 duplications, we cannot ru
125 26T>G in intron 30, with evidence supporting cosegregation with the disease in the family.
126 med transmission of the PIEZO1 mutations and cosegregation with the disease phenotype in all affected
127           Candidate variants were tested for cosegregation with the disease.
128  were screened and new variants assessed for cosegregation with the disease.
129 edicted to be damaging were investigated for cosegregation with the low HDL-C trait in the entire ext
130 c mutations and two of which exhibited exact cosegregation with the phenotype of interest.
131          Genetic mapping in pea demonstrated cosegregation with the yellow/green cotyledon polymorphi

 
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