Identification of a Testis-Specific Gene (C15orf2) in the Prader–Willi Syndrome Region on Chromosome 15
- 1 April 2000
- Vol. 65 (2) , 174-183
- https://doi.org/10.1006/geno.2000.6158
Abstract
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This publication has 53 references indexed in Scilit:
- The Host Defence Function of Genomic Methylation PatternsPublished by Wiley ,2007
- The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi RegionHuman Molecular Genetics, 1999
- The imprinting box of the mouse Igf2r geneNature, 1999
- Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal DiagnosisAmerican Journal of Human Genetics, 1998
- Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15Nature Genetics, 1995
- Spl elements protect a CpG island from de novo methylationNature, 1994
- Molecular definition of the Prader — Willi syndrome chromosome region and orientation of the SNRPN geneHuman Molecular Genetics, 1993
- Methylation patterns of testis-specific genes.Proceedings of the National Academy of Sciences, 1991
- CpG-rich islands and the function of DNA methylationNature, 1986
- ‘Puppet’ Children A Report on Three CasesDevelopmental Medicine and Child Neurology, 1965