The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader–Willi syndrome deletion region
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference18 articles.
1. Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brain;Aizawa;Dev. Brain Res.,1992
2. Oligodeoxyribonucleotide ligation to single-stranded cDNAs: a new tool for cloning 5′ ends of mRNAs and for constructing cDNA libraries by in vitro amplification;Edwards;Nucleic Acids Res.,1991
3. Parental-origin-specific epigenetic modification of the mouse H19 gene;Ferguson-Smith;Nature,1993
4. CpG islands in vertebrate genomes;Gardiner-Garden;J. Mol. Biol.,1987
5. Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene;Glenn;Am. J. Hum. Genet.,1996
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