The critical region for Angelman syndrome lies between D15S122 and D15S113
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference11 articles.
1. ‘Puppet’ Children A Report on Three Cases
2. Molecular definition of the Prader — Willi syndrome chromosome region and orientation of the SNRPN gene
3. Angelman syndrome associated with a maternal 15q11–13 deletion of less than 200 kb
4. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient
5. (1993): Mapping of the Angelman and Prader-Willi syndromes. In: (ed), “The Phenotypic Mapping of Down Syndrome and Other Aneuploid Conditions.” New York: Wiley-Liss pp 225-234.
Cited by 11 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. Molecular Mechanism of Angelman Syndrome in Two Large Families Involves an Imprinting Mutation;The American Journal of Human Genetics;1999-02
2. Mutation screening of the UBE3A /E6-AP gene in autistic disorder;Molecular Psychiatry;1999-01
3. Imprinting in Angelman and Prader-Willi syndromes;Current Opinion in Genetics & Development;1998-06
4. Genomic Organization of theUBE3A/E6-AP Gene and Related Pseudogenes;Genomics;1998-01
5. The elusive Angelman syndrome critical region.;Journal of Medical Genetics;1997-09-01
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