The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation (Q38509518)

3 September 2017

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation (English)

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3 September 2017

1

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Andrew Oliver Mungo Wilkie

3 September 2017

2

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3 September 2017

Buckle VJ

3

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3 September 2017

Winter RM

4

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3 September 2017

Holland AJ

5

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3 September 2017

McDermid HE

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3 September 2017

language of work or name

English

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publication date

1 February 1995

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3 September 2017

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3 September 2017

9

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3 September 2017

132-140

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3 September 2017

2

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https://scigraph.springernature.com/pub.10.1038/ng0295-132

3 September 2017

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cites work

Studies in mental handicap. I. Prevalence and distribution by clinical type and severity of defect

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

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

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Mild mental retardation in Swedish school children. I. Prevalence

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Mild mental retardation in Swedish school children. II. Etiologic and pathogenetic aspects.

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Aetiology of mild mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

The recurrence risks for mild idiopathic mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Systematic cloning of human minisatellites from ordered array charomid libraries.

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Human minisatellite alleles detectable only after PCR amplification

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

A systematic search for uniparental disomy in carriers of chromosome translocations

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Molecular heterogeneity of the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomere

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

A high-resolution cytogenetic map of human chromosome 3: localization of 291 new cosmid markers by direct R-banding fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Clustering of multiallele DNA markers near the Huntington's disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Characterization of a panel of highly variable minisatellites cloned from human DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

A highly polymorphic minisatellite (pMS627) on chromosome 14 (D14S44).

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements.

1 reference

https://api.crossref.org/works/10.1038%2FNG0295-132

7 January 2021

Identifiers

DOI

10.1038/NG0295-132

1 reference

3 September 2017

1 reference