Angelman syndrome associated with a maternal 15q11–13 deletion of less than 200 kb-Reference-Cited by-同舟云学术

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Angelman syndrome associated with a maternal 15q11–13 deletion of less than 200 kb

Published:1994 Issue:8 Volume:3 Page:1409-1413
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Buxton Jessica L.,Chan Chi-tsung J.,Gilbert Helen,Clayton-Smith Jill,Burn John,Pembrey Marcus,Malcolm Susan

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/8/1409/1473883/3-8-1409.pdf

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Towards an understanding of Angelman syndrome in mice studies;Journal of Neuroscience Research;2019-12-22

2. Angelman syndrome caused by an identical familial 1,487-kb deletion;American Journal of Medical Genetics Part A;2007-01-01

3. Gametic imprinting in development and disease;Journal of Endocrinology;1997-10-01

4. Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.;Journal of Medical Genetics;1997-08-01

5. Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman Syndromes;Arquivos de Neuro-Psiquiatria;1997-06

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