Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells-Reference-Cited by-同舟云学术

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

Published:2009-06-10 Issue:12 Volume:17 Page:1625-1634
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Bliek Jet,Alders Marielle,Maas Saskia M,Oostra Roelof-Jan,Mackay Deborah M,van der Lip Karin,Callaway Johnatan L,Brooks Alice,van 't Padje Sandra,Westerveld Andries,Leschot Nico J,Mannens Marcel MAM

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg200977.pdf

Reference44 articles.

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3. Wiedemann HR : Tumours and hemihypertrophy associated with Wiedemann Beckwith syndrome. Eur J Pediatr 1983; 141: 129.

4. Sotelo-Avila C, Gonzalez-Crussi F, Fowler JW : Complete and incomplete forms of Beckwith–Wiedemann syndrome: their oncogenic potential. J Pediatr 1980; 96: 47–50.

5. Pettenati MJ, Haines JL, Higgins RR et al: Wiedemann–Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Hum Genet 1986; 74: 143–154.

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