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Volumn 14, Issue 3, 1998, Pages 142-145

Meckel-Gruber syndrome

Author keywords

Encephalocele; Hydrocephaly; Meckel Gruber syndrome

Indexed keywords

ARTICLE; AUTOPSY; CASE REPORT; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE 46,XY; KIDNEY POLYCYSTIC DISEASE; MALE; MECKEL SYNDROME; NEWBORN; OUTCOMES RESEARCH; POLYDACTYLY; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0031863707     PISSN: 02567040     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003810050198     Document Type: Article
Times cited : (15)

References (11)
  • 1
    • 0025086847 scopus 로고
    • A distinctive triad of malformations of the central nervous system in the Meckel-Gruber syndrome
    • Ahdab-Barmada M, Claassen D (1960) A distinctive triad of malformations of the central nervous system in the Meckel-Gruber syndrome. J Neuropathol Exp Neurol 49:610-620
    • (1960) J Neuropathol Exp Neurol , vol.49 , pp. 610-620
    • Ahdab-Barmada, M.1    Claassen, D.2
  • 3
    • 0025394793 scopus 로고
    • Meckel-Gruber syndrome. A lethal combination of abnormalities
    • Coard KC, Escoffery CT (1990) Meckel-Gruber syndrome. A lethal combination of abnormalities. West Indian Med J 39:52-56
    • (1990) West Indian Med J , vol.39 , pp. 52-56
    • Coard, K.C.1    Escoffery, C.T.2
  • 7
    • 0029093126 scopus 로고
    • Current concept of hydrocephalus: Evolution of new classifications
    • Mori K (1995) Current concept of hydrocephalus: evolution of new classifications. Child's Nerv Syst 11:523-532
    • (1995) Child's Nerv Syst , vol.11 , pp. 523-532
    • Mori, K.1
  • 9
    • 0028980029 scopus 로고
    • The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24
    • Paavola P, Salonen R, Weissenbach J, Peltonen L (1995) The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24. Nat Genet 11:213-215
    • (1995) Nat Genet , vol.11 , pp. 213-215
    • Paavola, P.1    Salonen, R.2    Weissenbach, J.3    Peltonen, L.4
  • 10
    • 0019416725 scopus 로고
    • Phenotypic variation in Meckel syndrome
    • Seller MJ (1981) Phenotypic variation in Meckel syndrome. Clin Genet 20:74-77
    • (1981) Clin Genet , vol.20 , pp. 74-77
    • Seller, M.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.