Familial Hirschsprung's disease: Report of autosomal dominant and probable recessive X-linked kindreds
- 1 May 1991
- journal article
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 26 (5) , 591-594
- https://doi.org/10.1016/0022-3468(91)90714-5
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Familial Occurrence of Neuroblastoma, Von Recklinghausen's Neurofibromatosis, Hirschsprung's Agangliosis and Jaw‐winking SyndromeActa Paediatrica, 1989
- Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migration.Journal of Medical Genetics, 1988
- Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).Journal of Medical Genetics, 1988
- Three-generation transmission of Hirschsprung's diseaseClinical Genetics, 1987
- Hirschsprung disease: a genetic studyClinical Genetics, 1985
- Hirschsprung disease: Etiologic implications of unsuccessful prenatal diagnosisAmerican Journal of Medical Genetics, 1983
- Hirschsprungʼs Disease in a Family with Multiple Endocrine Neoplasia Type 2Journal of Pediatric Gastroenterology and Nutrition, 1982
- The association of Waardenburg syndrome and Hirschsprung megacolonAmerican Journal of Medical Genetics, 1979
- A family study of Hirschsprung's diseaseAnnals of Human Genetics, 1963
- HIRSCHSPRUNG'S DISEASEThe Lancet, 1951