Heritable Heteromorphism of the N. 16 Chromosome Pair in Man-Reference-Cited by-同舟云学术

Heritable Heteromorphism of the N. 16 Chromosome Pair in Man

Published:1969-01 Issue:1 Volume:18 Page:77-85
ISSN:1120-9623
Container-title:Acta geneticae medicae et gemellologiae
language:en
Short-container-title:Acta genet. med. gemellol.

Author:

Guanti G.,Balacco-Gabrieli C.,Battaglia E.

Abstract

SummaryA family is described with heteromorphism of N. 16 chromosome pair. The abnormal submetacentric chromosome was found in a total of 8 family members. Seven out of these carriers show a variable degree of myopia.

Publisher

Cambridge University Press (CUP)

Reference23 articles.

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2. Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease

3. Autosomal chromosome anomalies;Jennings;Med. J. Austral.,1961

4. Atypical acrocentric chromosomes in Negro and Caucasian mongols;Starkman;Amer. J. Hum. Genet.,1967

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