Evidence for the Role of PWCR1/HBII-85 C/D Box Small Nucleolar RNAs in Prader-Willi Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference30 articles.
1. A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression;Cattanach;Nat Genet,1992
2. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization;Cavaille;Proc Natl Acad Sci USA,2000
3. Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region;Cavaille;Hum Mol Genet,2002
4. Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome;Conroy;Am J Hum Genet,1997
5. Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain;de los Santos;Am J Hum Genet,2000
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