Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

about

The causes and consequences of random and non-random X chromosome inactivation in humans.CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy X-chromosome inactivation patterns in females with Prader-Willi syndrome.

P2860

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P2860

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

Item

http://www.wikidata.org/entity/Q41685594

description

1999 nî lūn-bûn

@nan

1999年の論文

@ja

1999年論文

@yue

1999年論文

@zh-hant

1999年論文

@zh-hk

1999年論文

@zh-mo

1999年論文

@zh-tw

1999年论文

@wuu

1999年论文

@zh

1999年论文

@zh-cn

name

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

@en

type

Item

label

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

@en

prefLabel

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

@en

P1476

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

@en

P2093

Baumer A

http://www.w3.org/2001/XMLSchema#string

Sun YJ

http://www.w3.org/2001/XMLSchema#string

P2860

Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation

Molecular heterogeneity of the fragile X syndrome.

A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication

Asynchronous DNA synthesis of sex chromatin in human interphase nuclei.

Characterization of the full fragile X syndrome mutation in fetal gametes.

Contribution of the FMR1 gene mutation to human intellectual dysfunction.

Molecular-neurobehavioral associations in females with the fragile X full mutation.

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

P304

162-164

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P31

scholarly article

P356

10.1002/(SICI)1096-8628(19990910)86:2<162::AID-AJMG14>3.0.CO;2-D

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

1999-09-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

10449653

http://www.w3.org/2001/XMLSchema#string

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

about

P2860

P2860

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698