Retinoblastoma and hirschsprung disease in a patient with interstitial deletion of chromosome 13

American Journal of Medical Genetics

Volumn 77, Issue 4, 1998, Pages 285-288

  Weigel, Brenda J ^a   Pierpont, Mary Ella M ^a   Young, Terri L ^b   Mutchler, Scott B ^c   Neglia, Joseph P ^a,b  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c UMHC ^*  (United States)

Author keywords

Chromosome 13; Hirschsprung disease; Retinoblastoma

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME DELETION 13; DISEASE CLASSIFICATION; HIRSCHSPRUNG DISEASE; HUMAN; INFANT; INTERSTITIAL CHROMOSOME DELETION; MALE; PRIORITY JOURNAL; RETINOBLASTOMA; SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 13; HIRSCHSPRUNG DISEASE; HUMANS; INFANT, NEWBORN; MALE; RETINOBLASTOMA;

EID: 0032557728     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980526)77:4<285::AID-AJMG7>3.0.CO;2-M     Document Type: Article

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