Imprinting in Prader-Willi and Angelman syndromes
Author:
Publisher
John Wiley & Sons, Ltd
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/047001153X.g103214/fullpdf
Reference72 articles.
1. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region;Boccaccio;Human Molecular Genetics,1999
2. Identification of novel exons 3��������� of the human SNRPN gene;Buiting;Genomics,1997
3. A candidate mouse model for Prader-Willi syndrome which shows an absence of SNRPN expression;Cattanach;Nature Genetics,1992
4. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19;DeBaun;American Journal of Human Genetics,2003
5. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13;Dittrich;Human Genetics,1992
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