10qter deletion: a new case.

Subjects

Subjects :

Child, Preschool
Craniofacial Abnormalities genetics
Humans
In Situ Hybridization, Fluorescence
Male
Monosomy
Oligonucleotide Array Sequence Analysis
Abnormalities, Multiple genetics
Chromosome Deletion
Chromosomes, Human, Pair 10 genetics
Developmental Disabilities genetics

Details

Language :

English

ISSN :

1552-4833

Volume :

146A

Issue :

18

Database :

MEDLINE

Journal :

American journal of medical genetics. Part A

Publication Type :

Academic Journal

Accession number :

18698621

Full Text :

https://doi.org/10.1002/ajmg.a.32467