Partial expression of Angelman syndrome in mother most likely to be due to mosaicism involving both somatic and germline cells-Reference-Cited by-同舟云学术

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Partial expression of Angelman syndrome in mother most likely to be due to mosaicism involving both somatic and germline cells

Published:1990-07 Issue:3 Volume:36 Page:369-369
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hall Judith G.

Publisher

Wiley

Subject

Genetics (clinical)

Reference3 articles.

1. Review aio! hypotheses: Somatic mosaicism: Observations related to clinical genetics;Hall;Am J Hum Genet,1988

2. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion;Knoll;Am J Med Genet,1989

3. Angelman syndrome in a daughter with del(l5)(qllq13) associated with brachycephaly, hearing loss, enlarged foramen magnum, and ataxia in the mother;Williams;Am J Med Genet,1989

Cited by 2 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. Mosaicism for deletion 17p11.2 in a boy with the Smith-Magenis syndrome;American Journal of Medical Genetics;1993-02-15

2. Normal and Pathologic Laughter in Children;Clinical Pediatrics;1991-11

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