A new genetic variant of the spinal muscular atrophies in infancy
about
The gene frequency of acute Werdnig-Hoffmann disease (SMA type 1). A total population survey in North-East EnglandNephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual associationHereditary distal spinal muscular atrophy with vocal cord paralysis.Diabetes mellitus, diabetes insipidus, and optic atrophy. An autosomal recessive syndrome?
P2860
A new genetic variant of the spinal muscular atrophies in infancy
description
1972 nî lūn-bûn
@nan
1972 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1972 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
name
A new genetic variant of the spinal muscular atrophies in infancy
@ast
A new genetic variant of the spinal muscular atrophies in infancy
@en
A new genetic variant of the spinal muscular atrophies in infancy
@nl
type
label
A new genetic variant of the spinal muscular atrophies in infancy
@ast
A new genetic variant of the spinal muscular atrophies in infancy
@en
A new genetic variant of the spinal muscular atrophies in infancy
@nl
prefLabel
A new genetic variant of the spinal muscular atrophies in infancy
@ast
A new genetic variant of the spinal muscular atrophies in infancy
@en
A new genetic variant of the spinal muscular atrophies in infancy
@nl
P2093
P1476
A new genetic variant of the spinal muscular atrophies in infancy
@en
P2093
Schneider HJ
Zellweger H
P2860
P304
P407
P577
1972-12-01T00:00:00Z