[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].

Subjects

Subjects :

Child
DNA Methylation
Humans
Intellectual Disability genetics
Male
Phenotype
Chromosomes, Human, Pair 15 genetics
Prader-Willi Syndrome genetics
Translocation, Genetic
X Chromosome Inactivation genetics

Details

Language :

Japanese

ISSN :

0029-0831

Volume :

46

Issue :

2

Database :

MEDLINE

Journal :

No to hattatsu = Brain and development

Publication Type :

Academic Journal

Accession number :

24738189