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PMID: 7211957 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

X-linked mental retardation: a study of 7 families.

American journal of medical genetics ·Vol. 7 ·No. 4 ·1980-00-00 ·Pages 471-89

Jacobs PA, Glover TW, Mayer M, Fox P, Gerrard JW, Dunn HG, Herbst DS

Abstract

Seven families with X-linked mental retardation (MR) have been studied clinically and cytogenetically. All affected males in six of the families were found to have a fragile site on Xq in a number of their peripheral lymphocytes. The fragile site was not seen in any of the affected males in the seventh family. The affected males in the six families with the fragile X had a syndrome characterized by a variable degree of MR, macro-orchidism, a characteristic repetitive, jocular speech, normal body proportions, and large jaws and ears. The fragile X chromosome could only be detected in a proportion of female carriers and its frequency in females was found to be correlated with their mental status to be inversely correlated with their age.

MeSH Terms
Adolescent Adult Aged Cells, Cultured Child Female Genetic Carrier Screening Genetic Linkage Humans Intellectual Disability/genetics Karyotyping Lymphocytes/ultrastructure Male Middle Aged Pedigree Sex Chromosomes/ultrastructure X Chromosome/ultrastructure
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Jacobs P A
Glover T W
Mayer M
Fox P
Gerrard J W
Dunn H G
Herbst D S
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1980-00-00
Pages
471-89
Language
English
Region
United States
NLM ID
7708900
Subset
IM
Grants
NICHD NIH HHS · HD 07879 · United States
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