Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.
about
Waardenburg syndromeHirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13.Hirschsprung disease, associated syndromes, and genetics: a review.Familiar hypopigmentation syndrome in sheep associated with homozygous deletion of the entire endothelin type-B receptor gene.Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.Therapeutic RNA interference of malignant melanoma by electrotransfer of small interfering RNA targeting Mitf.Mouse Dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud.Neural crest anomaly syndromes in children with spina bifida.
P2860
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P2860
Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.
description
1995 nî lūn-bûn
@nan
1995 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Chromosome 13q deletion with W ...... neural crest function on 13q.
@ast
Chromosome 13q deletion with W ...... neural crest function on 13q.
@en
type
label
Chromosome 13q deletion with W ...... neural crest function on 13q.
@ast
Chromosome 13q deletion with W ...... neural crest function on 13q.
@en
prefLabel
Chromosome 13q deletion with W ...... neural crest function on 13q.
@ast
Chromosome 13q deletion with W ...... neural crest function on 13q.
@en
P2093
P2860
P356
P1476
Chromosome 13q deletion with W ...... neural crest function on 13q.
@en
P2093
C T Baldwin
G Van Camp
L A Farrer
M Bonduelle
M N Van Thienen
P2860
P304
P356
10.1136/JMG.32.7.531
P407
P577
1995-07-01T00:00:00Z