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Volumn 49, Issue 1, 2003, Pages 29-44

Mental retardation: A review of the genetic causes

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; DISABILITY; ENVIRONMENTAL FACTOR; FRAGILE X SYNDROME; HEREDITY; HUMAN; INTELLIGENCE QUOTIENT; MENTAL DEFICIENCY; METABOLIC DISORDER; PREVALENCE; REVIEW; SKILL;

EID: 0037286976     PISSN: 09697950     EISSN: None     Source Type: Journal    
DOI: 10.1179/096979503799104138     Document Type: Review
Times cited : (33)

References (27)
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    • Amir, R.E., Van den Veyver, I.B., Wan, M., Tran, C.Q., Francke, U. and Zoghbi, H.Y. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics, 23, 185-188.
    • (1999) Nature Genetics , vol.23 , pp. 185-188
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  • 2
    • 0035464960 scopus 로고    scopus 로고
    • Monogenic causes of X-linked mental retardation
    • Chelly, J. and Mandel, J.L. (2001). Monogenic causes of X-linked mental retardation. Nature Reviews Genetics, 2, 669-80.
    • (2001) Nature Reviews Genetics , vol.2 , pp. 669-680
    • Chelly, J.1    Mandel, J.L.2
  • 7
    • 0035379735 scopus 로고    scopus 로고
    • The epidemiology of mental retardation of unknown cause
    • Croen L.A., Grether J.K. and Selvin S. (2001). The epidemiology of mental retardation of unknown cause. Pediatrics, 107, E86.
    • (2001) Pediatrics , vol.107
    • Croen, L.A.1    Grether, J.K.2    Selvin, S.3
  • 10
    • 0030137717 scopus 로고    scopus 로고
    • Identification of the gene FMR2, associated with FRAXE mental retardation
    • Gecz J., Gedeon A.K., Sutherland G.R. and Mulley J.C. (1996) Identification of the gene FMR2, associated with FRAXE mental retardation. Nature Genetics, 13, 105-108.
    • (1996) Nature Genetics , vol.13 , pp. 105-108
    • Gecz, J.1    Gedeon, A.K.2    Sutherland, G.R.3    Mulley, J.C.4
  • 12
    • 0036827032 scopus 로고    scopus 로고
    • High throughput screening of human subtelomeric DNA for copy number changes using mulitplex amplifiable probe hybridisation (MAPH)
    • Hollox E.J., Atia, T., Cross, G., Parkin, T. and Armour, J.A.L (2002). High throughput screening of human subtelomeric DNA for copy number changes using mulitplex amplifiable probe hybridisation (MAPH). Journal of Medical Genetics, 39, 790-795.
    • (2002) Journal of Medical Genetics , vol.39 , pp. 790-795
    • Hollox, E.J.1    Atia, T.2    Cross, G.3    Parkin, T.4    Armour, J.A.L.5
  • 18
    • 0036244955 scopus 로고    scopus 로고
    • The complex structure and dynamic evolution of human subtelomeres
    • Mefford H.C. and Trask B.J. (2002). The complex structure and dynamic evolution of human subtelomeres. Nature Reviews Genetics, 3, 91-102.
    • (2002) Nature Reviews Genetics , vol.3 , pp. 91-102
    • Mefford, H.C.1    Trask, B.J.2
  • 21
    • 0033518202 scopus 로고    scopus 로고
    • Genetics and general cognitive ability
    • Plomin, R. (1999) Genetics and general cognitive ability. Nature, 402 Suppl, C25-C29.
    • (1999) Nature , Issue.402 SUPPL.
    • Plomin, R.1
  • 22
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    • Rho proteins, mental retardation and the cellular basis of cognition
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    • Ramakers, G.J.1
  • 26
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    • Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: Is there a need for routine screening?
    • Winnepenninckx, B., Errijgers, V., Hayez-Delatte, E, Reyniers, E. and Kooy, R.F. (2002). Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: Is there a need for routine screening? Human Mutation, 20, 249-52.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.