Author:
Inbar-Feigenberg Michal,Choufani Sanaa,Cytrynbaum Cheryl,Chen Yi-An,Steele Leslie,Shuman Cheryl,Ray Peter N.,Weksberg Rosanna
Subject
Genetics(clinical),Genetics
Reference24 articles.
1. Paternal Uniparental Isodisomy of chromosome 20q-and the resulting changes in GNAS1 methylation-as a plausible cause of pseudohypoparathyroidism;Bastepe;Am J Hum Genet,2001
2. Bryke CR Garber AT Israel J 2004 Evolution of a complex phenotype in a unique patient with a paternal uniparental disomy for every chromosome cell line and a normal biparental inheritance cell line. [Abstract 831] http://www.ashg.org/genetics/ashg/annmeet/2004/menu-annmeet-2004.shtml
3. Genetic mosaicism in normal tissues of Wilms' tumour patients;Chao;Nat Genet,1993
4. Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray;Chen;Genomics,2011
5. Beckwith-Wiedemann syndrome;Choufani;Am J Med Genet Part C,2010
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