Heritability of X chromosome--inactivation phenotype in a large family.
about
Skewed X-chromosome inactivation in female carriers of dyskeratosis congenitaSex Chromosome Genetics '99. The X chromosome and recurrent spontaneous abortion: the significance of transmanifesting carriers.X-chromosome inactivation patterns in Korean women with idiopathic recurrent spontaneous abortion.Genetic localisation of mental retardation with spastic diplegia to the pericentromeric region of the X chromosome: X inactivation in female carriers.Comparison of X-chromosome inactivation patterns in multiple tissues from human females.Expression of the disease on female carriers of X-linked lysosomal disorders: a brief review.Inter- and intra-individual variation in allele-specific DNA methylation and gene expression in children conceived using assisted reproductive technology.Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.Commitment to X inactivation precedes the twinning event in monochorionic MZ twins.X chromosome inactivation in carriers of Barth syndrome.Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.Functional intergenic transcription: a case study of the X-inactivation centre.Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism.The dinucleotide repeat polymorphism in the 3'UTR of the CD154 gene has a functional role on protein expression and is associated with systemic lupus erythematosus.Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.Disseminated peritoneal leiomyomatosis. Clonality analysis by X chromosome inactivation and cytogenetics of a clinically benign smooth muscle proliferation.Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes.Skewing X chromosome choice by modulating sense transcription across the Xist locusNo evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans.Association of androgen receptor CAG repeat polymorphism and polycystic ovary syndromeX inactivation in females with X-linked Charcot-Marie-Tooth disease.Non-random X chromosome inactivation in Aicardi syndrome.Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.Genetic control of X inactivation and processes leading to X-inactivation skewing.Nonrandom X-chromosome inactivation in hemopoietic cells from carriers of dyskeratosis congenita.XIST expression and X-chromosome inactivation in human preimplantation embryos.Demonstration of a novel Xp22.2 microdeletion as the cause of familial extreme skewing of X-inactivation utilizing case-parent trio SNP microarray analysis.X-chromosome inactivation patterns in females with Prader-Willi syndrome.
P2860
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P2860
Heritability of X chromosome--inactivation phenotype in a large family.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Heritability of X chromosome--inactivation phenotype in a large family.
@ast
Heritability of X chromosome--inactivation phenotype in a large family.
@en
type
label
Heritability of X chromosome--inactivation phenotype in a large family.
@ast
Heritability of X chromosome--inactivation phenotype in a large family.
@en
prefLabel
Heritability of X chromosome--inactivation phenotype in a large family.
@ast
Heritability of X chromosome--inactivation phenotype in a large family.
@en
P2093
P2860
P1476
Heritability of X chromosome--inactivation phenotype in a large family.
@en
P2093
Naumova AK
Sapienza C
Willard HF
P2860
P304
P407
P577
1996-06-01T00:00:00Z