Fragile X syndrome

Research output: Contribution to journalArticle

57 Citations (Scopus)

Abstract

The fragile X syndrome is the most common inherited form of mental retardation known. Its phenotype includes large or prominent ears, macroorchidism, and characteristic behavioral problems. It has attracted the interest of cytogeneticists and molecular biologists because of its characteristic fragile site on the X chromosome. It has puzzled geneticists because of its unusual inheritance pattern involving nonpenetrant males. This syndrome has also spearheaded an appreciation of cytogenetic abnormalities in the etiology of all degrees of developmental delay.

Original languageEnglish (US)
Pages (from-to)626-674
Number of pages49
JournalCurrent Problems in Pediatrics
Volume17
Issue number11
DOIs
StatePublished - 1987
Externally publishedYes

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Fragile X Syndrome
Inheritance Patterns
X Chromosome
Chromosome Aberrations
Intellectual Disability
Ear
Phenotype
Problem Behavior

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Fragile X syndrome. / Hagerman, Randi J.

In: Current Problems in Pediatrics, Vol. 17, No. 11, 1987, p. 626-674.

Research output: Contribution to journalArticle

Hagerman, Randi J. / Fragile X syndrome. In: Current Problems in Pediatrics. 1987 ; Vol. 17, No. 11. pp. 626-674.
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