(Q34390532)

1 August 2017

title

The impact of transmission-ratio distortion on allele sharing in affected sibling pairs (English)

1 reference

1 August 2017

1 reference

2

Morgan K

1 reference

1 August 2017

Greenwood CM

1

1 reference

1 August 2017

language of work or name

English

0 references

publication date

20 April 2000

1 reference

American Journal of Human Genetics

1 August 2017

published in

1 reference

1 August 2017

volume

66

1 reference

1 August 2017

issue

6

1 reference

1 August 2017

page(s)

2001-2004

1 reference

A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Transmission-ratio distortion at Xp11.4-p21.1 in type 1 diabetes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

A genetic test to determine the origin of maternal transmission ratio distortion. Meiotic drive at the mouse Om locus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

The analysis of parental origin of alleles may detect susceptibility loci for complex disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Autism and the X chromosome. Multipoint sib-pair analysis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

The peculiar journey of a selfish chromosome: mouse t haplotypes and meiotic drive

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Linkage strategies for genetically complex traits. I. Multilocus models

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Transmission ratio distortion in females on chromosome 10p11-p15.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1378036

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10775526

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Transmission ratio distortion at the INS-IGF2 VNTR

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10775526

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/302918

1 reference

1 August 2017

1 reference

1 August 2017

1 reference