Cladistic structure within the human Lipoprotein lipase gene and its implications for phenotypic association studies. (Q34610913)

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1 November 2019

title

Cladistic structure within the human Lipoprotein lipase gene and its implications for phenotypic association studies (English)

1 reference

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1 November 2019

1 reference

4

E Boerwinkle

2 references

3 August 2017

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1 November 2019

author name string

A R Templeton

1

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1 November 2019

K M Weiss

2

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1 November 2019

D A Nickerson

3

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1 November 2019

C F Sing

5

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1 November 2019

language of work or name

English

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publication date

1 November 2000

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1 November 2019

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1 November 2019

volume

156

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1 November 2019

issue

3

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1 November 2019

page(s)

1259-1275

1 reference

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Recombinational and mutational hotspots within the human lipoprotein lipase gene

1 November 2019

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Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

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DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

7 July 2018

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7 July 2018

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Separating population structure from population history: a cladistic analysis of the geographical distribution of mitochondrial DNA haplotypes in the tiger salamander, Ambystoma tigrinum

7 July 2018

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Nonuniform recombination within the human beta-globin gene cluster

7 July 2018

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7 July 2018

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A cladistic analysis of phenotype associations with haplotypes inferred from restriction endonuclease mapping. II. The analysis of natural populations

7 July 2018

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7 July 2018

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7 July 2018

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Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene

7 July 2018

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Methylation, mutation and cancer

7 July 2018

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A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation

7 July 2018

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7 July 2018

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12 December 2020

Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome

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12 December 2020

The mutational demography of protein C deficiency

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12 December 2020

Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis

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12 December 2020

Identifiers

1 reference

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1 November 2019

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