Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs. - Wikidata - awgldk - TriplyDB

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

http://www.wikidata.org/entity/Q33902232

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When to suspect a genetic syndrome Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDH.48,XXYY in a General Adult Psychiatry Department.

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Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

http://www.wikidata.org/entity/Q33902232

description

2002 nî lūn-bûn

@nan

2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu

name

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

@ast

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

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type

label

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

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Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

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prefLabel

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

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Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

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Canadian Medical Association Journal

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Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs.

@en

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Alasdair G W Hunter

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P2860

Subtle chromosomal rearrangements in children with unexplained mental retardation

beta(1)-adrenergic antagonists improve sleep and behavioural disturbances in a circadian disorder, Smith-Magenis syndrome

Smith-Lemli-Opitz syndrome: a treatable inherited error of metabolism causing mental retardation.

Genetics 101: detecting mutations in human genes

Identifying people's genes: ethical aspects of DNA sampling in populations.

Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome.

Objective techniques for craniofacial assessment: what are the choices?

Outcome of the routine assessment of patients with mental retardation in a genetics clinic.

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367-372

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scholarly article

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4

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2002-08-01T00:00:00Z

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medical genetics

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