A candidate model for angelman syndrome in the mouse
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s003359900479.pdf
Reference40 articles.
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2. Beechey CV (1996) Maps of chromosome anomalies in the mouse. Mouse Genome 94, 74–96
3. Beechey CV, Ball S, Townsend S, Jones J (1997)The mouse Chromosome 7 distal imprinting domain maps to G bands F4/F5. Mamm Genome (in press)
4. Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B (1995) Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nature Genet 9, 395–400
5. Butler MG, Palmer CG (1983) Parental origin of chromosome 15 deletion in Prader-Willi syndrome. The Lancet I, 1285–1286
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