Chromosome abnormalities in Indonesian patients with short stature. - Wikidata - wikimedia - TriplyDB

Chromosome abnormalities in Indonesian patients with short stature.

Chromosome abnormalities in Indonesian patients with short stature.

http://www.wikidata.org/entity/Q34366175

about

Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.

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Chromosome abnormalities in Indonesian patients with short stature.

http://www.wikidata.org/entity/Q34366175

description

2012 nî lūn-bûn

@nan

2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

name

Chromosome abnormalities in Indonesian patients with short stature.

@ast

Chromosome abnormalities in Indonesian patients with short stature.

@en

Chromosome abnormalities in Indonesian patients with short stature.

@nl

type

label

Chromosome abnormalities in Indonesian patients with short stature.

@ast

Chromosome abnormalities in Indonesian patients with short stature.

@en

Chromosome abnormalities in Indonesian patients with short stature.

@nl

prefLabel

Chromosome abnormalities in Indonesian patients with short stature.

@ast

Chromosome abnormalities in Indonesian patients with short stature.

@en

Chromosome abnormalities in Indonesian patients with short stature.

@nl

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Molecular Cytogenetics

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Chromosome abnormalities in Indonesian patients with short stature.

@en

P2093

Alida Harahap

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

Chrysantine Paramayuda

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Debby D Ambarwati

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Hannie Kartapradja

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Helena W Anggaratri

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Lita P Suciati

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Nanis S Marzuki

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P2860

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature

Familial deletion 18p syndrome: case report

Jacobsen syndrome.

Mosaicism with a normal cell line and an autosomal structural rearrangement

Management of short stature.

Lesson of the week: Turner's syndrome mosaicism in patients with a normal blood lymphocyte karyotype.

Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype.

Delayed diagnoses of Turner's syndrome: proposed guidelines for change.

Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.

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35

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scholarly article

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10.1186/1755-8166-5-35

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1049167266

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