Frontonasal malformation with tetralogy of fallot associated with a submicroscopic deletion of 22q11

American Journal of Medical Genetics

Volumn 69, Issue 3, 1997, Pages 287-289

  Stratton, Robert F ^a   Payne, M ^a,b  

^a South Texas Genetics Center   (United States)

^b Central Texas Genetics Center   (United States)

Author keywords

bifid; deletion, 22q11; frontonasal dysplasia; nose; tetralogy of Fallot

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; DISEASE ASSOCIATION; FACE DEVELOPMENT; FACE MALFORMATION; FALLOT TETRALOGY; FEMALE; HUMAN; NOSE; NOSE MALFORMATION; PRESCHOOL CHILD; PRIORITY JOURNAL;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; INFANT, NEWBORN; NOSE; TETRALOGY OF FALLOT;

EID: 0031004202     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970331)69:3<287::AID-AJMG13>3.0.CO;2-N     Document Type: Article

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