Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome-Reference-Cited by-同舟云学术

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Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith–Wiedemann syndrome

Published:2001-06 Issue:6 Volume:9 Page:409-418
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Gaston Véronique,Le Bouc Yves,Soupre Véronique,Burglen Lydie,Donadieu Jeam,Oro Hubert,Audry Georges,Vazquez Marie-Paule,Gicquel Christine

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5200649.pdf

Reference33 articles.

1. Pettenati M, Haines J, Higgins R, Wappner R, Palmer C, Weaver D: Wiedemann–Beckwith syndrome: presentation of clinical, cytogenetic data on 22 new cases, review of the literature . Hum Genet 1986 74: 143–154

2. Elliot M, Maher E . Beckwith–Wiedemann syndrome J Med Genet 1994 31: 560–564

3. Li M, Squire J, Weksberg R . Molecular genetics of Wiedemann–Beckwith syndrome Am J Med Genet 1998 79: 253–259

4. Morison I, Becroft D, Taniguchi T, Woods C, Reeve A . Somatic overgrowth associated with overexpression of insulin-like growth factor II Nat Genet 1996 2: 311–316

5. Hoyme HE, Seaver LH, Jones KL, Procopio F, Crooks W, Feingold M . Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review Am J Med Genet 1998 79: 274–278

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