Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference50 articles.
1. Maternal uniparental disomy for chromosome 14;Temple;J Med Genet,1991
2. Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes;Kagami;Nat Genet,2008
3. Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity;Moon;Mol Cell Biol,2002
4. Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta;Sekita;Nat Genet,2008
5. The Dlk1 and Gtl2 genes are linked and reciprocally imprinted;Schmidt;Genes Dev,2000
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