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DNMT3B mutations and DNA methylation defect define two types of ICF syndrome

✍ Scribed by Y.L. Jiang; M. Rigolet; D. Bourc'his; F. Nigon; I. Bokesoy; J.P. Fryns; M. Hultén; P. Jonveaux; P. Maraschio; A. Mégarbané; A. Moncla; E. Viegas-Péquignot


Book ID
102263467
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
278 KB
Volume
25
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

✦ Synopsis


Communicated by Haig H


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