Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome

A male newborn with a ring 10 chromosome is described. The distal part of the long arm of chromosome 10, deleted during ring formation (10q25), is translocated to the short arm of chromosome 19.

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Bibliographic Details
Published in:Human genetics 1978-01, Vol.43 (2), p.239-244
Main Authors: Fryns, J P, De Boeck, K, Jaeken, J, van den Berghe, H
Format: Article
Language:English
Subjects:
Abnormalities, Multiple - genetics
Chromosome Aberrations
Chromosome Banding
Chromosome Disorders
Chromosomes, Human, 19-20
Chromosomes, Human, 6-12 and X
Craniofacial Dysostosis - genetics
Humans
Karyotyping
Translocation, Genetic
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Description
Summary:A male newborn with a ring 10 chromosome is described. The distal part of the long arm of chromosome 10, deleted during ring formation (10q25), is translocated to the short arm of chromosome 19.
ISSN:0340-6717
1432-1203
DOI:10.1007/BF00293602