Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1-Reference-Cited by-同舟云学术

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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

Published:2001-12-01 Issue:26 Volume:10 Page:2989-3000
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Weksberg R.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/10/26/2989/9813605/102989.pdf

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