Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
about
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndromeMouse and hamster mutants as models for Waardenburg syndromes in humans.Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.Genetic Screening in Patients with Craniofacial Malformations.SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.
P2860
Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase.
description
1989 nî lūn-bûn
@nan
1989 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Interstitial deletion of the l ...... s of isocitrate dehydrogenase.
@ast
Interstitial deletion of the l ...... s of isocitrate dehydrogenase.
@en
type
label
Interstitial deletion of the l ...... s of isocitrate dehydrogenase.
@ast
Interstitial deletion of the l ...... s of isocitrate dehydrogenase.
@en
prefLabel
Interstitial deletion of the l ...... s of isocitrate dehydrogenase.
@ast
Interstitial deletion of the l ...... s of isocitrate dehydrogenase.
@en
P2093
P2860
P356
P1476
Interstitial deletion of the l ...... ls of isocitrate dehydrogenase
@en
P2093
C A Swindlehurst
D A Aitken
P2860
P304
P356
10.1136/JMG.26.2.127
P407
P577
1989-02-01T00:00:00Z