(Q34390482)

1 August 2017

Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22. (English)

1 reference

1 August 2017

5

1 reference

1 August 2017

B Yuan

1

1 reference

1 August 2017

R Neuman

2

1 reference

1 August 2017

S H Duan

3

1 reference

1 August 2017

J L Weber

4

1 reference

1 August 2017

N L Saccone

6

1 reference

1 August 2017

J S Wu

7

1 reference

1 August 2017

K Y Liu

8

1 reference

1 August 2017

G Schonfeld

9

1 reference

1 August 2017

language of work or name

English

0 references

publication date

10 April 2000

1 reference

American Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

66

1 reference

1 August 2017

1699-1704

1 reference

1 August 2017

5

1 reference

Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Multipoint quantitative-trait linkage analysis in general pedigrees

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Parametric and nonparametric linkage analysis: a unified multipoint approach

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Reference intervals for plasma apolipoprotein B determined with a standardized commercial immunoturbidimetric assay: results from the Framingham Offspring Study.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

The hypobetalipoproteinemias

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Faster sequential genetic linkage computations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Cholesterol and mortality. 30 years of follow-up from the Framingham study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Evidence for a dominant gene that suppresses hypercholesterolemia in a family with defective low density lipoprotein receptors

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Apolipoprotein B gene mutations affecting cholesterol levels

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Known mutations of apoB account for only a small minority of hypobetalipoproteinemia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Asymptomatic elevation of aminotransferase levels and fatty liver secondary to heterozygous hypobetalipoproteinemia

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

Genetic heterogeneity in familial hypobetalipoproteinemia: linkage and non-linkage to the apoB gene in Caucasian families.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378026

A form of familial hypobetalipoproteinaemia not due to a mutation in the apolipoprotein B gene

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10762553

12 December 2020

inferred from PubMed ID database lookup

Fatty liver in heterozygous hypobetalipoproteinemia caused by a novel truncated form of apolipoprotein B

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10762553

12 December 2020

inferred from PubMed ID database lookup

Frequency of ApoB and ApoE Gene Mutations as Causes of Hypobetalipoproteinemia in the Framingham Offspring Population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10762553

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1086/302904

1 reference

release_atkf3urdcvfdvj5pnhsk3d75lq

1 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/atkf3urdcvfdvj5pnhsk3d75lq

24 November 2022

mapped directly with Wikidata item

PMCID

1378026

1 reference

1 August 2017

1 reference