Identification of Novel Imprinted Transcripts in the Prader-Willi Syndrome and Angelman Syndrome Deletion Region: Further Evidence for Regional Imprinting Control
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference62 articles.
1. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints;Amos-Landgraf;Am J Hum Genet,1999
2. Competition—a common motif for the imprinting mechanism?;Barlow;EMBO J,1997
3. dbEST—database for “expressed sequence tags”;Boguski;Nat Genet,1993
4. ESTablishing a human transcript map;Boguski;Nat Genet,1995
5. Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations;Browne;Am J Hum Genet,1997
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