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Volumn 6, Issue 1, 1996, Pages 35-36

The role of genetics in understanding hydrocephahis and spina bifida. An update

Author keywords

[No Author keywords available]

Indexed keywords

CHILD; CONFERENCE PAPER; GENETICS; HUMAN; HYDROCEPHALUS; MOUSE; MUTATION; NONHUMAN; SPINA BIFIDA;

EID: 0030473514     PISSN: 09396764     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (13)
  • 1
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    • A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mud signs of Waardenburg syndrome
    • Hol F, Hamel B, Geurds M, Mullaart R, Barr F, Marina R, Mariman E: A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mud signs of Waardenburg syndrome. J Med Genet 32 (1995) 52-56
    • (1995) J Med Genet , vol.32 , pp. 52-56
    • Hol, F.1    Hamel, B.2    Geurds, M.3    Mullaart, R.4    Barr, F.5    Marina, R.6    Mariman, E.7
  • 2
    • 4243459140 scopus 로고
    • Molecular genetics of hydrocephalus - Fine structural mapping of the congenital hydrocephalns (ch) mouse mutant
    • Hong H, Chakravarti A. Molecular genetics of hydrocephalus - Fine structural mapping of the congenital hydrocephalns (ch) mouse mutant Am J Hum Genet 57 (4 SS) (1995) 756
    • (1995) Am J Hum Genet , vol.57 , Issue.4 SS , pp. 756
    • Hong, H.1    Chakravarti, A.2
  • 3
    • 0023113381 scopus 로고
    • Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP)
    • Jones H, Dack S, Ellis C: Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP). Acta Neuropathol (Berl) 72 (1987) 268-276
    • (1987) Acta Neuropathol (Berl) , vol.72 , pp. 268-276
    • Jones, H.1    Dack, S.2    Ellis, C.3
  • 4
    • 0030029134 scopus 로고    scopus 로고
    • X-linked hydrocephalus and MASA syndrome
    • Kenwrick S, Jouet M, Donnai D: X-linked hydrocephalus and MASA syndrome. J Med Genet 33 (1996) 59-65
    • (1996) J Med Genet , vol.33 , pp. 59-65
    • Kenwrick, S.1    Jouet, M.2    Donnai, D.3
  • 5
    • 0019427490 scopus 로고
    • A new model of congenital hydrocephalus in the rat
    • Kohn D, Chinookoswong N, Chou S: A new model of congenital hydrocephalus in the rat. Acta Neuropathol 54 (1981) 211-218
    • (1981) Acta Neuropathol , vol.54 , pp. 211-218
    • Kohn, D.1    Chinookoswong, N.2    Chou, S.3
  • 6
    • 0022312729 scopus 로고
    • Congenital genetic murine (ch) hydrocephalus
    • Richardson R: Congenital genetic murine (ch) hydrocephalus. Child's Nerv Syst 1 (1985) 87-99
    • (1985) Child's Nerv Syst , vol.1 , pp. 87-99
    • Richardson, R.1
  • 7
    • 84970061068 scopus 로고
    • Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus
    • Rosenthal A, Jouet M, Kenwrick S: Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus. Nature Genet 2 (1992) 107-112
    • (1992) Nature Genet , vol.2 , pp. 107-112
    • Rosenthal, A.1    Jouet, M.2    Kenwrick, S.3
  • 9
    • 0029932086 scopus 로고    scopus 로고
    • Transcription factor AP-2 essential for cranial closure and cramofacial development
    • Schorle H, Meier P, Buchert M, Jaenisch R, Mitchell P: Transcription factor AP-2 essential for cranial closure and cramofacial development Nature 381 (1996) 235-238
    • (1996) Nature , vol.381 , pp. 235-238
    • Schorle, H.1    Meier, P.2    Buchert, M.3    Jaenisch, R.4    Mitchell, P.5
  • 11
    • 0030034268 scopus 로고    scopus 로고
    • Relevance to spina bifida of mutated methylenetetrahydrofolate reductase
    • Wilcken D, Wang X: Relevance to spina bifida of mutated methylenetetrahydrofolate reductase. Lancet 347 (1996) 340
    • (1996) Lancet , vol.347 , pp. 340
    • Wilcken, D.1    Wang, X.2
  • 13
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    • Familial hydrocephalus of prenatal onset
    • Zlotogora J, Sagi M, Cohen T: Familial hydrocephalus of prenatal onset Am J Med Genet 49 (1994) 202-204
    • (1994) Am J Med Genet , vol.49 , pp. 202-204
    • Zlotogora, J.1    Sagi, M.2    Cohen, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.