Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 Deletion, including a familial case [4]

American Journal of Medical Genetics

Volumn 79, Issue 5, 1998, Pages 406-410

  Bawle, E V ^a   Conard, J ^a   Van Dyke, D L ^a   Czarnecki, P ^a   Driscoll, D A ^a  

^a CHILDREN'S HOSPITAL OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART DISEASE; FACE MUSCLE; LETTER; MUSCLE MALFORMATION; PREVALENCE; PRIORITY JOURNAL;

ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FACIAL MUSCLES; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MOUTH ABNORMALITIES; SYNDROME;

EID: 0032511756     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19981012)79:5<406::AID-AJMG18>3.0.CO;2-V     Document Type: Letter

References (8)