A further case of monosomy 10qter.

Clinical genetics ·Vol. 24 ·No. 3 ·1983-12-20

Evans-Jones G, Walker S, Howard P J

Abstract

A child with a terminal deletion of chromosome 10 (q26) is described. A comparison of the phenotypic and cytogenetic features is made in the five reported cases of monosomy 10qter. No phenotypic features are found sufficiently characteristic to delineate a syndrome. Enzymatic activities for PGAMA and GOT1 were normal.

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

0009-9163

Published

1983-12-20

Indexed

1983-12-20

Updated

2016-11-23

Language

English

Country/Region

Denmark

NLM ID

0253664

External Links

PubMed source View journal details

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A further case of monosomy 10qter.

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