Parental origin of the extra chromosome in the cat eye syndrome: Evidence from heteromorphism and in situ hybridization analysis-Reference-Cited by-同舟云学术

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Parental origin of the extra chromosome in the cat eye syndrome: Evidence from heteromorphism and in situ hybridization analysis

Published:1988-01 Issue:1 Volume:29 Page:9-19
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Magenis R. E.,Sheehy R. R.,Brown M. G.,McDermid H. E.,White B. N.,Zonana J.,Weleber R.,Optiz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference32 articles.

1. Localization of heterochromatin in human chromosomes

2. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

3. Identification of human chromosomes by DNA-binding fluorescent agents

4. A deletion in chromosome 22 can cause digeorge syndrome

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