The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Author:

Jay Philippe,Rougeulle Claire,Massacrier Annick,Moncla Anne,Mattel Marie-Geneviève,Malzac Perrine,Roëckel Nathalie,Taviaux Sylvie,Bergé Lefranc Jean-Louis,Cau Pierre,Berta Philippe,Lalande Marc,Muscatelli Françoise

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference31 articles.

1. Nicholls, R.D., Knoll, J.H.M., Butler, M.G., Karam, S. & Lalande, M. Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome. Nature. 342, 281–285 (1989).

2. Robinson, W.P. et al. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. Am. J. Hum. Genet. 49, 1219–1234 (1991).

3. Mascari, M.J. et al. Molecular diagnosis of Prader-Willi syndrome. N. Engl. J. Med. 326, 1599–1607 (1992).

4. Holm, V., Cassidy, S., Butler, M., Hanchett, J. & Greenberg, F. Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics. 91, 398–402 (1993).

5. Lalande, M. Parental imprinting and human disease. Annu. Rev. Genet. 30, 173–195 (1997).

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