Angelman Syndrome: Molecular Cytogenetic Studies

J Gordon Millichap

doi:10.15844/pedneurbriefs-11-2-10

Angelman Syndrome: Molecular Cytogenetic Studies

Pediatric Neurology Briefs

Volume 11 (1997): Issue 2

By: J Gordon Millichap

Open Access

|Feb 1997

Abstract

Clinical, neurological, and molecular genetic studies of 22 patients with diagnostic features of Angelman syndrome (AS) are reported from National Taiwan University Hospital, Taipei.

References

Hou J-W Wang P-J Wang T-R Angelman syndrome assessed by neurological and molecular cytogenetic investigations Pediatr Neurol 1997 Jan 16 1 17 22 10.1016/S0887-8994(96)00264-0 9044396
Open DOI Search in Google Scholar Back to article

Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-11-2-10 | Journal eISSN: 2166-6482

Journal RSS Feed

Language: English

Page range: 15 - 15

Published on: Feb 1, 1997

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Angelman Syndrome,

Fluorescence in Situ Hybridization,

Ataxic Cerebral Palsy

© 1997 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 11 (1997): Issue 2