Are moment bounds on the recombination fraction between a marker and a disease locus too good to be true? Allelic association mapping revisited for simple genetic diseases in the Finnish population (Q35644114)

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scientific article published on December 1995

Language	Label	Description	Also known as
English	Are moment bounds on the recombination fraction between a marker and a disease locus too good to be true? Allelic association mapping revisited for simple genetic diseases in the Finnish population	scientific article published on December 1995

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scholarly article

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

Are moment bounds on the recombination fraction between a marker and a disease locus too good to be true? Allelic association mapping revisited for simple genetic diseases in the Finnish population (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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2

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B S Weir

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Europe PubMed Central

PMC publication ID

14 October 2019

author name string

N L Kaplan

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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publication date

1 December 1995

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14 October 2019

American Journal of Human Genetics

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

57

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

6

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1486-1498

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801420

12 July 2018

Disease gene mapping in isolated human populations: the example of Finland

1 reference

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The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6

1 reference

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Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19

1 reference

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1 reference

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Genetic dissection of complex traits

1 reference

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An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21

1 reference

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High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene.

1 reference

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Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses

1 reference

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The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

1 reference

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Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes

1 reference

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Likelihood methods for locating disease genes in nonequilibrium populations.

1 reference

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1 reference

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Measuring the strength of associations between HLA antigens and diseases

1 reference

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Identification of the cystic fibrosis gene: genetic analysis

1 reference

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12 July 2018

A second-generation linkage map of the human genome

1 reference

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Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes

1 reference

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The Huntington's disease candidate region exhibits many different haplotypes

1 reference

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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

1 reference

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27 July 2018

Haplotype analysis to determine the position of a mutation among closely linked DNA markers

1 reference

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12 December 2020

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8533779%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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