Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
about
Identification of three novel NHS mutations in families with Nance-Horan syndromeLinkage analysis of Norrie disease with X-chromosomal ornithine aminotransferaseA novel NHS mutation causes Nance-Horan Syndrome in a Chinese family.Hereditary pediatric cataract on the Arabian Peninsula.Ophthalmic pathology of Nance-Horan syndrome: case report and review of the literature.Congenital diaphragmatic hernia as a part of Nance-Horan syndrome?
P2860
Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.
description
1989 nî lūn-bûn
@nan
1989 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հունվարին 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
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@ast
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@en
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@nl
type
label
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@ast
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@en
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@nl
prefLabel
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@ast
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@en
Mapping the gene for X-linked ...... l of the Nance-Horan syndrome.
@nl
P2860
P1476
Mapping the gene for X-linked ...... al of the Nance-Horan syndrome
@en
P2093
P2860
P304
P577
1989-01-01T00:00:00Z