Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus
about
X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia.X-linked mental retardation: in pursuit of a gene map.
P2860
Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus
description
1973 nî lūn-bûn
@nan
1973 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1973 թվականի մարտին հրատարակված գիտական հոդված
@hy
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
name
Possible linkage between Xg an ...... with or without hydrocephalus
@ast
Possible linkage between Xg an ...... with or without hydrocephalus
@en
Possible linkage between Xg an ...... with or without hydrocephalus.
@nl
type
label
Possible linkage between Xg an ...... with or without hydrocephalus
@ast
Possible linkage between Xg an ...... with or without hydrocephalus
@en
Possible linkage between Xg an ...... with or without hydrocephalus.
@nl
prefLabel
Possible linkage between Xg an ...... with or without hydrocephalus
@ast
Possible linkage between Xg an ...... with or without hydrocephalus
@en
Possible linkage between Xg an ...... with or without hydrocephalus.
@nl
P1476
Possible linkage between Xg an ...... with or without hydrocephalus
@en
P2093
P407
P577
1973-03-01T00:00:00Z