[1p36 microdeletion syndrome].

Subjects

Subjects :

Abnormalities, Multiple diagnosis
Chromosome Deletion
Chromosome Disorders diagnosis
Chromosomes, Human, Pair 1
Humans
Infant
Intellectual Disability diagnosis
Male
Phenotype
Syndrome
Abnormalities, Multiple genetics
Intellectual Disability genetics

Details

Language :

Spanish; Castilian

ISSN :

1695-9531

Volume :

74

Issue :

3

Database :

MEDLINE

Journal :

Anales de pediatria (Barcelona, Spain : 2003)

Publication Type :

Report

Accession number :

21315668

Full Text :

https://doi.org/10.1016/j.anpedi.2010.09.033