Molecular mechanisms in Angelman syndrome: a survey of 93 patients.

Author:

Chan C T,Clayton-Smith J,Cheng X J,Buxton J,Webb T,Pembrey M E,Malcolm S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference39 articles.

1. Further evidence for dominant inheritance at the chromosome 15ql 113 locus in familial Angelman syndrome;Clayton-Smith, J.; Webb, T.; Robb, S.A.;AmJMed Genet,1992

2. DNA deletion and its parental origin in Angelman syndrome patients;Hamabe, J.; Kuroki, Y.; Imaizumi, K.;Am J Med Genet,1991

3. 'Puppet' children: a report of three cases;Angelman, H.;Dev Med Child Neurol,1965

4. Angelman syndrome;Clayton-Smith, J.; Pembrey, M.E.;7 Med Genet,1992

5. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons;Williams, C.A.; Gray, B.A.; Hendrickson, J.E.; Stone, J.W.; Cantu, E.S.;Am J Med Genet,1989

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