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

J P Fryns; K De Boeck; J Jaeken; H van den Berghe

doi:10.1007/BF00293602

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

Hum Genet. 1978 Aug 31;43(2):239-44. doi: 10.1007/BF00293602.

Authors

J P Fryns, K De Boeck, J Jaeken, H van den Berghe

PMID: 567620
DOI: 10.1007/BF00293602

Abstract

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.

MeSH terms

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*