Genomic imprinting in disruptive spermatogenesis
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Genomic imprinting: parental influence on the genome;Reik;Nat Rev Genet,2001
2. Rare congenital disorders, imprinted genes, and assisted reproductive technology;Gosden;Lancet,2003
3. Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis;Kerjean;Hum Mol Genet,2000
4. Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer;Takai;Hum Mol Genet,2001
5. A potential imprint control element. Identification of a conserved 42 bp sequence upstream of H19.;Frevel;Trends Genet,1999
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