(Q28305514)

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Homozygosity mapping at Alström syndrome to chromosome 2p

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Homozygosity mapping at Alström syndrome to chromosome 2p (English)

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G B Collin

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J D Marshall

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L R Cardon

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P M Nishina

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language of work or name

English

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publication date

February 1997

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published in

Human Molecular Genetics

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volume

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issue

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page(s)

213-9

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cites work

Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy

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21 January 2018

Impaired insulin-induced RNA synthesis secondary to a genetically defective insulin receptor.

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Familial hypercholesterolemia in French-Canadians: taking advantage of the presence of a "founder effect".

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21 January 2018

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

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21 January 2018

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

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21 January 2018

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

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21 January 2018

A patient with features of both Bardet-Biedl and Alström syndromes

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reference URL

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21 January 2018

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

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21 January 2018

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

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21 January 2018

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

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21 January 2018

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity

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21 January 2018

Chromosomal localization of the beta-adducin gene to mouse chromosome 6 and human chromosome 2

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Chromosomal mapping of the human annexin IV (ANX4) gene

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21 January 2018

Physical mapping of the human glutamine:fructose-6-phosphate amidotransferase gene (GFPT) to chromosome 2p13

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21 January 2018

The gene for human transforming growth factor alpha is on the short arm of chromosome 2.

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21 January 2018

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

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A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands

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21 January 2018

Identifiers

DOI

10.1093/HMG/6.2.213

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PubMed publication ID

9063741

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ResearchGate publication ID

14147816

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