(Q28138252)

1

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R Regan

2

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A Nicod

3

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S W Horsley

4

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L Kearney

5

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T Homfray

6

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R M Winter

7

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P Bolton

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

8

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language of work or name

English

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publication date

13 November 1999

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published in

The Lancet

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volume

354

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issue

9191

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page(s)

1676-81

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cites work

1 reference

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7 January 2021

An etiological survey of the severely retarded Hertfordshire children who were born between January 1, 1965 and December 31, 1967

1 reference

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7 January 2021

Aetiology of mild mental retardation

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7 January 2021

The recurrence risks for mild idiopathic mental retardation

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

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7 January 2021

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

1 reference

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7 January 2021

Characterization of short tandem repeats from thirty-one human telomeres

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Cytogenetic survey of a hospital for the mentally retarded

1 reference

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7 January 2021

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

1 reference

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7 January 2021

DNA testing for fragile X syndrome in schools for learning difficulties

1 reference

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7 January 2021

Population studies of the fragile X: a molecular approach

1 reference

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7 January 2021

Fragile X syndrome is less common than previously estimated

1 reference