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Volumn 6, Issue 11, 1996, Pages 1396-1398

Human genetics: Dissecting Williams syndrome

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EID: 0030294803     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-9822(96)00740-3     Document Type: Article
Times cited : (17)

References (15)
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  • 4
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    • The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis
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    • Curran, M.E.1    Atkinson, D.L.2    Ewart, A.K.3    Morris, C.A.4    Leppart, M.F.5    Keating, M.T.6
  • 8
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    • Deletions of the elastin gene at 7q11.23 occur in 90% of patients with Williams syndrome
    • Nickerson E, Greenberg F, Keating MT, McCaskill C, Shaffer LG: Deletions of the elastin gene at 7q11.23 occur in 90% of patients with Williams syndrome. Am J Hum Genet 1995, 56:1156-1161.
    • (1995) Am J Hum Genet , vol.56 , pp. 1156-1161
    • Nickerson, E.1    Greenberg, F.2    Keating, M.T.3    McCaskill, C.4    Shaffer, L.G.5
  • 9
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    • Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice
    • Grant SGN, O'Dell TJ, Karl KA, Stein PL, Soriano P, Kandel ER: Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice. Science 1992, 258:1903-1910.
    • (1992) Science , vol.258 , pp. 1903-1910
    • Grant, S.G.N.1    O'Dell, T.J.2    Karl, K.A.3    Stein, P.L.4    Soriano, P.5    Kandel, E.R.6
  • 11
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    • Albeliovich A, Chen C, Goda Y, Silva AJ, Stevens CF, Tonegawa S: Modified hippocampal long-term potentiation in PKCγ mutant mice. Cell 1993, Cell 75:1253-1262.
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    • PKCγ mutant mice exhibit mild deficits in spatial and contextual learning
    • Albeliovich SF, Paylor R, Chen C, Kim JJ, Wehner JM, Tonegawa S: PKCγ mutant mice exhibit mild deficits in spatial and contextual learning. Cell 1993, 75:1263-1271.
    • (1993) Cell , vol.75 , pp. 1263-1271
    • Albeliovich, S.F.1    Paylor, R.2    Chen, C.3    Kim, J.J.4    Wehner, J.M.5    Tonegawa, S.6
  • 13
    • 0028335706 scopus 로고
    • Identification of a human cDNA encoding a novel protein kinase with two repeats of the LIM/double zinc finger motif
    • Mizuno K, Okano I, Ohashi K, Nunoue K, Kuma K, Miyata T, Nakamura T: Identification of a human cDNA encoding a novel protein kinase with two repeats of the LIM/double zinc finger motif. Oncogene 1994, 9:1605-1612.
    • (1994) Oncogene , vol.9 , pp. 1605-1612
    • Mizuno, K.1    Okano, I.2    Ohashi, K.3    Nunoue, K.4    Kuma, K.5    Miyata, T.6    Nakamura, T.7
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    • Kiz-1, a protein with LIM zinc finger and kinase domains, is expressed mainly in neurons
    • Bernard O, Ganiatsas S, Kannourakis G, Dringen R: Kiz-1, a protein with LIM zinc finger and kinase domains, is expressed mainly in neurons. Cell Growth Differentiation 1994, 5:1159-1171.
    • (1994) Cell Growth Differentiation , vol.5 , pp. 1159-1171
    • Bernard, O.1    Ganiatsas, S.2    Kannourakis, G.3    Dringen, R.4
  • 15
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    • Position effects and genetic disease
    • Milot E, Fraser P, Grosveld F: Position effects and genetic disease. Trends Genet 1996, 12:123-126.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.