Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.
about
Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortiumWaardenburg syndrome and myelomeningocele in a family.Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1)Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7.
P2860
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.
description
1991 nî lūn-bûn
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1991 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@ast
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@en
type
label
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@ast
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@en
prefLabel
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@ast
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@en
P2093
P2860
P1476
Waardenburg syndrome (WS): the ...... arkers on human chromosome 2q.
@en
P2093
P2860
P407
P577
1991-01-01T00:00:00Z