Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.
about
Prader-Willi syndrome and mosaic Turner's syndrome.Patients with mosaic methylation patterns of the Prader-Willi/Angelman Syndrome critical region exhibit AS-like phenotypes with some PWS featuresMosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP array.A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
P2860
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.
description
1997 nî lūn-bûn
@nan
1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@ast
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@en
type
label
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@ast
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@en
prefLabel
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@ast
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@en
P2093
P2860
P356
P1476
Prader-Willi syndrome in a chi ...... riplo-X: a molecular analysis.
@en
P2093
Cassiman JJ
Devriendt K
Matthijs G
Proesmans W
P2860
P304
P356
10.1136/JMG.34.4.318
P407
P577
1997-04-01T00:00:00Z