Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders-Reference-Cited by-同舟云学术

Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders

Published:2009-12-09 Issue:5 Volume:19 Page:803-814
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Demars Julie,Shmela Mansur Ennuri,Rossignol Sylvie,Okabe Jun,Netchine Irène,Azzi Salah,Cabrol Sylvie,Le Caignec Cédric,David Albert,Le Bouc Yves,El-Osta Assam,Gicquel Christine

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/19/5/803/13926849/ddp549.pdf

Reference41 articles.

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2. Epigenetic deregulation of imprinting in congenital diseases of aberrant growth;Delaval;Bioessays,2006

3. Hormonal regulation of fetal growth;Gicquel;Horm. Res.,2006

4. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome;Gaston;Eur. J. Hum. Genet.,2001

5. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome;Cooper;Eur. J. Hum. Genet.,2005

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