The 22q11.2 deletion syndrome.

Advances in pediatrics

Volumn 48, Issue , 2001, Pages 39-73

  Emanuel, B S ^a   McDonald McGinn, D ^a   Saitta, S C ^a   Zackai, E H ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; DIGEORGE SYNDROME; FEMALE; GENETICS; HUMAN; INFANT; MALE; MULTIPLE MALFORMATION SYNDROME; PHENOTYPE; PRESCHOOL CHILD; REVIEW;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HUMANS; INFANT; MALE; PHENOTYPE;

EID: 0035224560     PISSN: 00653101     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (107)