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Volumn 32, Issue 5, 1997, Pages 724-727

Hirschsprung's disease in Oman

Author keywords

consanguinity; genetics; Hisrschsprung's disease; incidence; Oman

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 10; CONSANGUINEOUS MARRIAGE; ENVIRONMENTAL FACTOR; ENVIRONMENTAL TEMPERATURE; FEMALE; GENETIC PREDISPOSITION; HIRSCHSPRUNG DISEASE; HUMAN; INCIDENCE; INFANT; MAJOR CLINICAL STUDY; MALE; MYENTERIC PLEXUS; OMAN; PEDIATRIC SURGERY; POPULATION RESEARCH; PRIORITY JOURNAL; TERATOGENICITY;

EID: 0030970575     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3468(97)90015-4     Document Type: Article
Times cited : (26)

References (19)
  • 2
    • 84981776731 scopus 로고
    • A family study of Hirschsprung's disease
    • Bodian M, Carter CO: A family study of Hirschsprung's disease. J Med Genet 26:261-277, 1963
    • (1963) J Med Genet , vol.26 , pp. 261-277
    • Bodian, M.1    Carter, C.O.2
  • 3
    • 0014210694 scopus 로고
    • The genetics of Hirschsprung's disease: Evidence for heterogeneous etiology and a study of sixty three families
    • Passarge E: The genetics of Hirschsprung's disease: Evidence for heterogeneous etiology and a study of sixty three families. N Engl J Med 276:138-143, 1967
    • (1967) N Engl J Med , vol.276 , pp. 138-143
    • Passarge, E.1
  • 4
    • 0021970463 scopus 로고
    • Hirschsprungs disease in a large birth cohort
    • Spouge D, Baird PA: Hirschsprungs disease in a large birth cohort. Teratology 32:171-177, 1985
    • (1985) Teratology , vol.32 , pp. 171-177
    • Spouge, D.1    Baird, P.A.2
  • 5
    • 0027185569 scopus 로고
    • A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10
    • Lyonnet S, Bolino A, Pelet A, et al: A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. Nature Genet 4:346-348, 1994
    • (1994) Nature Genet , vol.4 , pp. 346-348
    • Lyonnet, S.1    Bolino, A.2    Pelet, A.3
  • 6
    • 0028618372 scopus 로고
    • A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
    • Puffenberger EG, Hosoda K, Washington SS, et al: A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease. Cell 79:1257-1266, 1994
    • (1994) Cell , vol.79 , pp. 1257-1266
    • Puffenberger, E.G.1    Hosoda, K.2    Washington, S.S.3
  • 8
    • 0024617477 scopus 로고
    • No correlation between hypertermia during pregnancy and Hirschprung's disease in the offspring
    • Larson LT, Okmian L, Kristafferson UN: No correlation between hypertermia during pregnancy and Hirschprung's disease in the offspring. (Letter) Am J Med Genet 32:260-261, 1989
    • (1989) Am J Med Genet , vol.32 , pp. 260-261
    • Larson, L.T.1    Okmian, L.2    Kristafferson, U.N.3
  • 9
    • 0001316449 scopus 로고
    • A simple exact test for birth order effect
    • Haldane JBS, Smith CAB: A simple exact test for birth order effect. Ann Eugen 14:117-124, 1947
    • (1947) Ann Eugen , vol.14 , pp. 117-124
    • Haldane, J.B.S.1    Smith, C.A.B.2
  • 11
    • 0021732114 scopus 로고
    • An epidemiological study of Hirschsprung's disease
    • Goldberg EL: An epidemiological study of Hirschsprung's disease. Int J Epidemiol 13:479-485, 1984
    • (1984) Int J Epidemiol , vol.13 , pp. 479-485
    • Goldberg, E.L.1
  • 12
    • 0028203639 scopus 로고
    • An epidemiological study of Hirschsprung's disease and additional anomalies
    • Russell MB, Russell CA, Niebuhr E: An epidemiological study of Hirschsprung's disease and additional anomalies. Acta Paed 83.68-71, 1994
    • (1994) Acta Paed , vol.83 , pp. 68-71
    • Russell, M.B.1    Russell, C.A.2    Niebuhr, E.3
  • 13
    • 0021344732 scopus 로고
    • Diagnosis and treatment of Hirschprung's disease in Japan
    • Ikeda K, Goto S: Diagnosis and treatment of Hirschprung's disease in Japan. Ann Surg 4:400-405, 1994
    • (1994) Ann Surg , vol.4 , pp. 400-405
    • Ikeda, K.1    Goto, S.2
  • 16
    • 0019406679 scopus 로고
    • White forelock, pigmentary disorders of the irides and long segment Hirschsprung disease: Possible variant of Waardenburg disease
    • Shah KN, Dalal SJ, Desai MP, et al: White forelock, pigmentary disorders of the irides and long segment Hirschsprung disease: Possible variant of Waardenburg disease. J Pediatr 99:432-435, 1981
    • (1981) J Pediatr , vol.99 , pp. 432-435
    • Shah, K.N.1    Dalal, S.J.2    Desai, M.P.3
  • 17
    • 12644288436 scopus 로고
    • Endothelin B receptor gene mutation in a consangineous family with Waardenberg-Hirschsprung Disease: A possible variant of Waardenberg disease
    • Attie T, Till M, Amiel J, et al: Endothelin B receptor gene mutation in a consangineous family with Waardenberg-Hirschsprung Disease: A possible variant of Waardenberg disease. J Pediatr 99:432-435, 1981
    • (1981) J Pediatr , vol.99 , pp. 432-435
    • Attie, T.1    Till, M.2    Amiel, J.3
  • 18
    • 0024576097 scopus 로고
    • Interstitial deletion of distal 13q associated with Hirschsprung's disease
    • Lamont MA, Fitchett M, Dennis NR: Interstitial deletion of distal 13q associated with Hirschsprung's disease. J Med Genet 26:100-104, 1979
    • (1979) J Med Genet , vol.26 , pp. 100-104
    • Lamont, M.A.1    Fitchett, M.2    Dennis, N.R.3
  • 19
    • 0025944896 scopus 로고
    • A case of Hirschprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): Potential mapping of one disease locus
    • Bottani A, Xie Y, Binkert F, et al: A case of Hirschprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): Potential mapping of one disease locus. Hum Genet 87:748-750, 1991
    • (1991) Hum Genet , vol.87 , pp. 748-750
    • Bottani, A.1    Xie, Y.2    Binkert, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.