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PMID: 1126048 Published · ppublish English Journal Article

Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

Clinical genetics ·Vol. 7 ·No. 4 ·1975-04-00 ·Pages 261-73

Blank CE, Colver DC, Potter AM, McHugh J, Lorber J

Abstract

A family with the reciprocal translocation t(9;22)(q13;q11) segregating in genetically balanced and unbalanced form is identified. The clinical features of four members with trisomy for the short arm of 9, and the proximal part of the long arm of 9, are described in detail. Features in common are summarized and compared with developmental abnormality observed in other examples of trisomy for the short arm of 9. An attempt is made to delineate further the clinical features commonly seen in trisomy for the short arm of 9.

MeSH Terms
Adult Child Chromosomes, Human, 6-12 and X Dermatoglyphics Female Humans Intellectual Disability/genetics Karyotyping Pedigree Translocation, Genetic Trisomy
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Blank C E
Colver D C
Potter A M
McHugh J
Lorber J
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1975-04-00
Pages
261-73
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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