Clinical Genetics · 1986 · 25 citations · 23 references
Life SciencesGeneticsPediatricsCytogeneticsHuman GeneticsPediatric GeneticsChildren With DisabilitiesChromosomal AbnormalitiesGenetic DisordersGenetic SyndromesNeurodevelopmental DisordersNeurodevelopmental GeneticsConstitutional Chromosome AbnormalitiesFragile SitesHuman Intelligence
The frequency of rare fragile sites was studied among 240 children in special schools for subnormal intelligence (IQ 52-85). 1/130 boys studied (0.8%) had the fragile site at Xq27.3 while it was not found in any girl (0/110). In two children an autosomal rare fragile site at 2q11.2 (2/240, 0.8%) was seen. In addition a constitutional chromosome abnormality was found in a further seven children (7/240, 2.9%).
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The marker (X) syndrome: a cytogenetic and genetic analysis
Stephanie L. Sherman, N.E. Morton, P. A. Jacobs et al. · Annals of Human Genetics · 1984 · 389 citations
X‐linked mental retardation: A study of 7 families
Patricia A. Jacobs, Thomas W. Glover, Patricia G Fox et al. · American Journal of Medical Genetics · 1980 · 211 citations