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Article

[Spread of X-chromosome inactivation into chromosome 15 is associated with Prader Willi syndrome phenotype in a boy with a t (X ; 15) (p21.1 ; q11.2) translocation].

No to hattatsu = Brain and development - 1 Mar 2014

Sakazume Satoru

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Share to Child
Share to Chromosomes, Human, Pair 15
Share to DNA Methylation
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Prader-Willi Syndrome

Share to Translocation, Genetic

Share to X Chromosome Inactivation

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PMID: 24738189

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Related research

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Research trail→

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[Spread of X-chromosome inactivation into chromosome 15 is associated with Prader Willi syndrome phenotype in a boy with a t (X ; 15) (p21.1 ; q11.2) translocation].PMID 24738189Read ↗

Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).Semantic proximity Read ↗

Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.Semantic proximity Read ↗

Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature.Semantic proximity Read ↗

[Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].Semantic proximity Read ↗

A Y/15 translocation in a 45,X male with Prader-Willi syndrome.Semantic proximity Read ↗

Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation.Semantic proximity Read ↗

Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.Semantic proximity Read ↗

Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.Semantic proximity Read ↗

An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13.Semantic proximity Read ↗

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.Semantic proximity Read ↗

[Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].Semantic proximity Read ↗

Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.Semantic proximity Read ↗

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