Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region.

Ning Y, Roschke A, Christian SL, Lesser J, Sutcliffe JS, Ledbetter DH
Genome Res. 1996 6 (8): 742-6

PMID: 8858349 · DOI:10.1101/gr.6.8.742

MeSH Terms (8)

Chromosome Mapping DNA, Complementary Genome, Human Humans Molecular Sequence Data Prader-Willi Syndrome Ribonucleoproteins, Small Nuclear Transcription, Genetic

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