Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland (Q55671005)

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16 September 2022

population genetics

1 reference

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16 September 2022

linkage disequilibrium

1 reference

6

E Lander

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Albert de la Chapelle

2

object named as

A de la Chapelle

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author name string

J. Hästbacka

1

1 reference

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16 September 2022

I. Kaitila

3

1 reference

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16 September 2022

P. Sistonen

4

1 reference

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A. Weaver

5

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng1192-204

16 September 2022

language of work or name

English

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publication date

November 1992

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published in

Nature Genetics

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volume

2

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page(s)

204-11

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issue

3

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exact match

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cites work

Positional cloning: let's not call it reverse anymore

1 reference

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Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

21 January 2018

1 reference

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Tandem linkage of human CSF-1 receptor (c-fms) and PDGF receptor genes

21 January 2018

1 reference

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Human c-fms proto-oncogene: comparative analysis with an abnormal allele

21 January 2018

1 reference

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Mapping complex genetic traits in humans: new methods using a complete RFLP linkage map

21 January 2018

1 reference

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7 January 2021

Identification of the cystic fibrosis gene: genetic analysis

1 reference

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7 January 2021

The Finnish population structure A genetic and genealogical study

1 reference

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7 January 2021

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1 reference

7 January 2021

Diastrophic dysplasia gene maps to the distal long arm of chromosome 5

1 reference

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7 January 2021

A linkage map spanning the locus for diastrophic dysplasia (DTD).

1 reference

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7 January 2021

On the distributions of frequencies of mutation to genes determining harmful traits in man

1 reference

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7 January 2021

Variances and covariances of squared linkage disequilibria in finite populations

1 reference

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7 January 2021

Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: application to aspartylglucosaminuria in Finland

1 reference

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7 January 2021

High prevalence of aspartylglycosaminuria among school-age children in eastern Finland

1 reference

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7 January 2021

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

1 reference

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7 January 2021

Restriction fragment length polymorphism of the human c-fms gene

1 reference

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7 January 2021

Dinucleotide repeat polymorphism at the human c-fms proto-oncogene for the CFS-1 receptor (CFS1R)

1 reference

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7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/NG1192-204

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1049816422

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