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Stormy J. Chamberlain et al.
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Prader-Willi syndrome
Suzanne B. Cassidy et al.
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A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
Adam J. de Smith et al.
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Prader-Willi phenotype caused by paternal deficiency for the HBII-85C/D box small nucleolar RNA cluster
Trilochan Sahoo et al.
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C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain
Karin Buiting et al.
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Angelman syndrome 2005: Updated consensus for diagnostic criteria
CA Williams et al.
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Regulation of the large (∼1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn
M Landers et al.
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Promoter-restricted H3 Lys 4 di-methylation is an epigenetic mark for monoallelic expression
C Rougeulle et al.
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The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A
M Runte et al.
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The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a
SJ Chamberlain et al.
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Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
J Cavaillé et al.
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