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PMID: 6851223 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The fragile X chromosome in a large Indian kindred.

Clinical genetics ·Vol. 23 ·No. 4 ·1983-04-00 ·Pages 311-7

Gardner RJ, Smart RD, Cornell JM, Merckel LM, Beighton P

Abstract

A large Indian kindred in which the fragile X chromosome is segregating has been investigated in Cape Town. Eight male hemizygotes and four female heterozygotes were mentally retarded. There is suggestive evidence that one deceased male of reportedly normal intelligence may have been a hemizygote. The existence of the fragile X syndrome in a number of different ethnic groups supports the contention that the gene controlling the phenotype and the fragile site are the same, or at least overlap.

MeSH Terms
Adolescent Adult Child Child, Preschool Female Fragile X Syndrome/genetics,pathology,psychology Heterozygote Humans India/ethnology Intelligence Male Middle Aged Pedigree Sex Chromosome Aberrations/genetics South Africa Testis/pathology
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Gardner R J
Smart R D
Cornell J M
Merckel L M
Beighton P
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1983-04-00
Pages
311-7
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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