A further case of monosomy 10qter

descriptionPublicationkeyboard_double_arrow_right Article 01 Sep 1983 English Publisher:WileyJournal:Clinical Genetics, volume 24, pages 216-219 (issn: 0009-9163, eissn: 1399-0004,

Authors: G, Evans-Jones; S, Walker; P J, Howard;

doi: 10.1111/j.1399-0004.1983.tb02242.x

pmid: 6194924

A further case of monosomy 10qter

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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 GOTl were normal.

Related Organizations

Liverpool Hospital
Australia

Keywords

Chromosomes, Human, 6-12 and X, Male, Phosphoglycerate Mutase, Developmental Disabilities, Humans, Infant, Aspartate Aminotransferases, Chromosome Deletion

8 Research products, page 1 of 1

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