about
Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.A prospective observational study of associated anomalies in Hirschsprung's disease.USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.Letter: Hirschsprung's disease and congenital deafness.
P2860
description
1973 nî lūn-bûn
@nan
1973年の論文
@ja
1973年論文
@yue
1973年論文
@zh-hant
1973年論文
@zh-hk
1973年論文
@zh-mo
1973年論文
@zh-tw
1973年论文
@wuu
1973年论文
@zh
1973年论文
@zh-cn
name
Hirschsprung's disease and congenital deafness.
@en
type
label
Hirschsprung's disease and congenital deafness.
@en
prefLabel
Hirschsprung's disease and congenital deafness.
@en
P2860
P356
P1476
Hirschsprung's disease and congenital deafness
@en
P2093
P2860
P304
P356
10.1136/JMG.10.4.337
P407
P577
1973-12-01T00:00:00Z