Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s

American Journal of Medical Genetics

Volumn 91, Issue 5, 2000, Pages 351-354

  Wenger, Sharon L ^c   Boone, Leslie Y ^a   Cummins, James H ^a   Del Vecchio, Maria A ^a   Bay, Carolyn A ^a,b   Hummel, Marybeth ^c   Mowery Rushton, Patricia A ^a  

^a CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^b UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

^c WEST VIRGINIA UNIVERSITY   (United States)

Author keywords

22qter deletion; Anal atresia; Fluorescence in situ hybridization; Velocardiofacial syndrome

Indexed keywords

ANUS ATRESIA; ARTICLE; CASE REPORT; CHROMOSOME 22; CHROMOSOME DELETION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; NEWBORN; PRIORITY JOURNAL; RING CHROMOSOME; VELOCARDIOFACIAL SYNDROME;

ABNORMALITIES, MULTIPLE; ANUS, IMPERFORATE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FACE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; RING CHROMOSOMES; SYNDROME;

EID: 0034709203     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000424)91:5<351::AID-AJMG6>3.0.CO;2-A     Document Type: Article

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