Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.

Author:

Langlois S,Yong S L,Wilson R D,Kwong L C,Kalousek D K

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome;Nicholls, R.D.; Knoll, J.H.M.; Butler, M.G.; Karam, S.; Lalande, M.;Nature,1989

2. cytogenetic and clinical investigations of Prader-Willi syndrome patients;Robinson, W.P.; Bottani, A.; Yagang, X.;Am J Hum Genet,1991

3. The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis;Mascari, M.J.; Gottlieb, W.; Rogan, P.K.;N Engl J Med,1992

4. Uniparental paternal disomy in Angelman's syndrome;Malcolm, S.; Clayton-Smith, J.; Nichols, M.;Lancet,1991

5. Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 robertsonian translocation carrier. Am 3 Hum Genet;Wang, J.C.C.; Passage, M.B.; Yen, P.H.; Shapiro, L.J.; Mohandas, T.K.,1991

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