Subtle chromosomal rearrangements in children with unexplained mental retardation (Q28138252)

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R Regan

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A Nicod

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S W Horsley

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L Kearney

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T Homfray

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R M Winter

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P Bolton

Severe Mental Retardation in a Swedish County – II. Etiologic and Pathogenetic Aspects of Children Born 1959–1970

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publication date

13 November 1999

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language of work or name

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354

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issue

9191

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page(s)

1676-81

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cites work

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Aetiology of mild mental retardation

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The recurrence risks for mild idiopathic mental retardation

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Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease

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The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

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A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration

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Characterization of short tandem repeats from thirty-one human telomeres

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

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Molecular-cytogenetic detection of a deletion of 1p36.3.

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Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs

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Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports

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Chromosome testing in children with developmental delay in whom the aetiology is not evident clinically.

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Cytogenetic survey of a hospital for the mentally retarded

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A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti institution, Finland

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DNA testing for fragile X syndrome in schools for learning difficulties

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Population studies of the fragile X: a molecular approach

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Fragile X syndrome is less common than previously estimated

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