FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes-Reference-Cited by-同舟云学术

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FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes

Published:1996-03-29 Issue:3 Volume:62 Page:216-223
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Teshima I.,Chadwick D.,Chitayat D.,Kobayashi J.,Ray P.,Shuman C.,Siegel-Bartelt J.,Strasberg P.,Weksberg R.

Publisher

Wiley

Subject

Genetics (clinical)

Reference41 articles.

1. FISH analysis in Prader-Willi and Angelman syndrome patients

2. Molecular study of chromosome 15 in 22 patients with Angelman syndrome

3. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

4. High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome

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. Genetics and Drug Discovery;Drug Discovery and Development;2021

2. Prader-Willi syndrome with a cleft palate: A case report;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2020-05

3. Three siblings with Prader–Willi syndrome caused by imprinting center microdeletions and review;American Journal of Medical Genetics Part A;2018-02-13

4. Familial Prader-Willi syndrome: case report and a literature review;Clinical Genetics;2000-09

5. Submicroscopic deletion in cousins with Prader‐Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting;American Journal of Medical Genetics;2000-04-25

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