Chromosome 22q11 deletion and pachygyria characterized by array-based comparative genomic hybridization.

American journal of medical genetics. Part A

Volumn 131, Issue 3, 2004, Pages 322-324

  Koolen, David A ^a   Veltman, Joris A ^a   Renier, Willy O ^a   Droog, Richard P ^a   van Kessel, Ad Geurts ^a   de Vries, Bert B A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN CORTEX; CASE REPORT; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; CONGENITAL MALFORMATION; DNA MICROARRAY; FEMALE; HUMAN; INFANT; NOTE; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEIC ACID HYBRIDIZATION;

CEREBRAL CORTEX; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;

MLCS; MLOWN;

EID: 21644485012     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30377     Document Type: Note

References (0)