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Volumn 29, Issue 12, 2013, Pages 2151-2155

Mowat-Wilson syndrome: The first report of an association with central nervous system tumors

Author keywords

Brain cancer; Cancer genetics; Children; Hirschsprung's disease; Mowat Wilson syndrome

Indexed keywords

CISPLATIN; LOMUSTINE; PHENOBARBITAL; TEMOZOLOMIDE; VINCRISTINE;

EID: 84890517306     PISSN: 02567040     EISSN: 14330350     Source Type: Journal    
DOI: 10.1007/s00381-013-2283-5     Document Type: Article
Times cited : (15)

References (9)
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    • Galloway, T.J.1    Indelicato, D.J.2    Amdur, R.J.3    Swanson, E.L.4    Morris, C.G.5    Marcus, R.B.6
  • 7
    • 33645380163 scopus 로고    scopus 로고
    • The contribution of associated congenital anomalies in understanding Hirschsprung's disease
    • 16518596 10.1007/s00383-006-1655-2 1:STN:280:DC%2BD287nvVCktw%3D%3D
    • Moore SW (2006) The contribution of associated congenital anomalies in understanding Hirschsprung's disease. Pediatr Surg Int 22(4):305-315
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    • Moore, S.W.1
  • 8
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    • Hirschsprung's disease and the brain
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    • Moore SW (2011) Hirschsprung's disease and the brain. Pediatr Surg Int 27(4):347-352
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    • Moore, S.W.1
  • 9
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    • Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: Delineation of a new syndrome and identification of a locus at chromosome 2q22-q23
    • 9719364 10.1136/jmg.35.8.617 1:STN:280:DyaK1czotlyluw%3D%3D
    • Mowat DR, Croaker GD, Cass DT, Kerr BA, Chaitow J, Adès LC, Chia NL, Wilson MJ (1998) Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. J Med Genet 35(8):617-623
    • (1998) J Med Genet , vol.35 , Issue.8 , pp. 617-623
    • Mowat, D.R.1    Croaker, G.D.2    Cass, D.T.3    Kerr, B.A.4    Chaitow, J.5    Adès, L.C.6    Chia, N.L.7    Wilson, M.J.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.