Familial deletions of chromosome 22q11: The Leuven experience [3]

American Journal of Medical Genetics

Volumn 80, Issue 5, 1998, Pages 531-532

  Swillen, A ^a   Devriendt, K ^a   Vantrappen, G ^a   Vogels, A ^a   Rommel, N ^a   Fryns J , P ^a   Eyskens, B ^a   Gewillig, M ^a   Dumoulin, M ^a  

^a CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22Q; CHROMOSOME DELETION; FAMILIAL DISEASE; HUMAN; LETTER; MAJOR CLINICAL STUDY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

BELGIUM; BIAS (EPIDEMIOLOGY); CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; MALE; PHENOTYPE;

EID: 0032545207     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19981228)80:5<531::AID-AJMG20>3.0.CO;2-L     Document Type: Letter

References (5)