Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.
about
Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease geneCoffin-Lowry syndrome: clinical and molecular features.Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome.X linked retinoschisis.Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors.
P2860
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2.
description
1992 nî lūn-bûn
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1992 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1992年の論文
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1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
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name
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@ast
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@en
type
label
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@ast
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@en
prefLabel
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@ast
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@en
P2093
P2860
P1476
Confirmation and refinement of ...... yndrome locus in Xp22.1-p22.2.
@en
P2093
Biancalana V
Gilgenkrantz S
Schinzel A
P2860
P304
P407
P577
1992-05-01T00:00:00Z