(Q35248025)

7 August 2017

The detection of linkage and heterogeneity in nuclear families for complex disorders: one versus two marker loci (English)

1 reference

7 August 2017

Martinez MM

1

1 reference

PubMed ID

2929598

7 August 2017

Goldin LR

series ordinal

2

1 reference

PubMed ID

2929598

7 August 2017

language of work or name

English

0 references

publication date

1 April 1989

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

44

1 reference

7 August 2017

4

1 reference

7 August 2017

552-559

1 reference

The number of families required to detect or exclude linkage heterogeneity

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715576

Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715576

Power and robustness of the linkage homogeneity test in genetic analysis of common disorders.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715576

Power of the affected-sib-pair method for heterogeneous disorders.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715576

Strategies for studying heterogeneous genetic traits in humans by using a linkage map of restriction fragment length polymorphisms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715576

Strategies for multilocus linkage analysis in humans

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715576

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2929598

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2929598

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic analysis workshop IV: summary of two-point and multipoint mapping of 11p

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2929598

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1715576

1 reference

7 August 2017

1 reference

PubMed ID

2929598