Familial Hirschsprung's disease: 20 cases in 12 kindreds.

[1]  F. Rescorla,et al.  Hirschsprung's Disease: Evaluation of Mortality and Long-term Function in 260 Cases , 1992 .

[2]  G. Besner,et al.  Familial Hirschsprung's disease: report of autosomal dominant and probable recessive X-linked kindreds. , 1991, Journal of pediatric surgery.

[3]  J. Hall,et al.  Genomic imprinting: review and relevance to human diseases. , 1990, American journal of human genetics.

[4]  A. Chakravarti,et al.  A genetic study of Hirschsprung disease. , 1990, American journal of human genetics.

[5]  A. Lipson,et al.  Three‐generation transmission of Hirschsprung's disease , 1987, Clinical genetics.

[6]  P. Kiss,et al.  Association of 13q deletion and Hirschsprung's disease. , 1989, Journal of medical genetics.

[7]  N. Tommerup,et al.  Familial Occurrence of Neuroblastoma, Von Recklinghausen's Neurofibromatosis, Hirschsprung's Agangliosis and Jaw‐winking Syndrome , 1989, Acta paediatrica Scandinavica.

[8]  N. Dennis,et al.  Interstitial deletion of distal 13q associated with Hirschsprung's disease. , 1989, Journal of medical genetics.

[9]  J. Hall,et al.  Review and hypotheses: somatic mosaicism: observations related to clinical genetics. , 1988, American journal of human genetics.

[10]  G. Webb,et al.  Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22). , 1988, Journal of medical genetics.

[11]  A. Lipson,et al.  Hirschsprung disease in the offspring of mothers exposed to hyperthermia during pregnancy. , 1988, American journal of medical genetics.

[12]  J. C. Law,et al.  Hirschsprung disease: a genetic study , 1985, Clinical genetics.

[13]  P. Baird,et al.  Hirschsprung disease in a large birth cohort. , 1985, Teratology.

[14]  Y. Takada,et al.  The association of imperforate anus and Hirschsprung's disease in siblings. , 1985, Journal of pediatric surgery.

[15]  James G. Chandler,et al.  Familial Hirschsprung's disease and type D brachydactyly: a report of four affected males in two generations. , 1983, Pediatrics.

[16]  M. Gadd,et al.  Hirschsprung's disease in a kindred: a possible clue to the genetics of the disease. , 1982, Journal of pediatric surgery.

[17]  M. Verdy,et al.  Hirschsprung's disease in a family with multiple endocrine neoplasia type 2. , 1982, Journal of pediatric gastroenterology and nutrition.

[18]  G. Omenn,et al.  The association of Waardenburg syndrome and Hirschsprung megacolon. , 1979, American journal of medical genetics.

[19]  J. Grosfeld,et al.  A critical evaluation of the Duhamel operation for Hirschsprung's disease. , 1978, Archives of surgery.

[20]  A. Mackinnon,et al.  Total intestinal aganglionosis. An autosomal recessive condition? , 1977, Archives of disease in childhood.

[21]  J. H. Fisher,et al.  Diagnosis of congenital megacolon: an analysis of 501 patients. , 1973, Journal of pediatric surgery.

[22]  E. Passarge.  The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families. , 1967, The New England journal of medicine.

[23]  M. Bodian,et al.  A family study of Hirschsprung's disease , 1963 .