about
Renpenning syndrome maps to Xp11.Non-specific X linked mental retardation.Fragile X chromosome: clinical and cytogenetic studies on cases from seven families.Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.Fragile X chromosome and X-linked mental retardation.Recombinant DNA approach to X-linked mental retardation.Absence of the fragile X in a group of patients with idiopathic mental retardation.X-linked mental retardation: in pursuit of a gene map.X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21.Further delineation of X-linked mental retardation.The Martin-Bell-Renpenning syndrome.
P2860
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P2860
description
1980 nî lūn-bûn
@nan
1980 թուականին հրատարակուած գիտական յօդուած
@hyw
1980 թվականին հրատարակված գիտական հոդված
@hy
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
name
X-linked mental retardation: Renpenning revisited
@ast
X-linked mental retardation: Renpenning revisited
@en
X-linked mental retardation: Renpenning revisited
@nl
type
label
X-linked mental retardation: Renpenning revisited
@ast
X-linked mental retardation: Renpenning revisited
@en
X-linked mental retardation: Renpenning revisited
@nl
prefLabel
X-linked mental retardation: Renpenning revisited
@ast
X-linked mental retardation: Renpenning revisited
@en
X-linked mental retardation: Renpenning revisited
@nl
P2093
P356
P1476
X-linked mental retardation: Renpenning revisited
@en
P2093
P356
10.1002/AJMG.1320070409
P407
P577
1980-01-01T00:00:00Z