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Volumn 40, Issue 1, 2003, Pages 62-64

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART) [5]

Author keywords

[No Author keywords available]

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; EMBRYO CULTURE; GENE CLUSTER; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HISTORY OF MEDICINE; HUMAN; IN VITRO STUDY; LETTER; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0037238396     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (528)

References (22)
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  • 2
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    • Beckwith-Wiedemann syndrome
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    • Elliott, M.1    Maher, E.R.2
  • 6
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    • Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19 independent pathway. Hum Mol Genet 1996;6:2027-32.
    • (1996) Hum Mol Genet , vol.6 , pp. 2027-2032
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  • 8
    • 0033609117 scopus 로고    scopus 로고
    • Loss of imprinting of a paternally expressed transcript, with antisense orientation to KCNQ1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
    • Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KCNQ1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc Natl Acad Sci USA 1999;96:5203-8.
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    • in press
    • Clayton-Smith J, Laan LAEM. Angelman syndrome: a review of the clinical and genetic aspects. J Med Genet (in press).
    • J Med Genet
    • Clayton-Smith, J.1    Laan, L.A.E.M.2
  • 13
    • 0028939902 scopus 로고
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    • Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet 1995;94:395-400.
    • (1995) Nat Genet , vol.94 , pp. 395-400
    • Buiting, K.1    Saitoh, S.2    Gross, S.3    Dittrich, B.4    Schwartz, S.5    Nicholls, R.D.6    Horsthemke, B.7
  • 16
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    • (2001) Hum Reprod , vol.16 , pp. 1588-1591
    • Olivennes, F.1    Fanchin, R.2    Ledee, N.3    Righini, C.4    Kadoch, U.5    Frydman, R.6
  • 18
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    • Adult phenotype in the mouse can be affected by epigenetic events in the early embryo
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  • 20
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    • Dean W, Bowden L, Aitchison A, Klose J, Moore T, Meneses JJ, Reik W, Feil R. Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes. Development 1998;125:2273-82.
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    • Dean, W.1    Bowden, L.2    Aitchison, A.3    Klose, J.4    Moore, T.5    Meneses, J.J.6    Reik, W.7    Feil, R.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.