Low frequency of inherited deletions of 22q11 [2]

American Journal of Medical Genetics

Volumn 85, Issue 5, 1999, Pages 513-514

  Smith, A ^a   Robson, L ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME DELETION; DIGEORGE SYNDROME; FAMILIAL INCIDENCE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; LETTER; PRIORITY JOURNAL; VELOCARDIOFACIAL SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; GENETIC DISEASES, INBORN; GENETIC MARKERS; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; SYNDROME; VELOPHARYNGEAL INSUFFICIENCY;

EID: 0033609920     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990827)85:5<513::AID-AJMG16>3.0.CO;2-J     Document Type: Letter

References (9)