Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. (Q34385627)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9585588%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

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

1 reference

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11 November 2019

author name string

M Leppert

series ordinal

2

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11 November 2019

D F Barker

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9585588%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

C Sapienza

series ordinal

5

1 reference

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11 November 2019

language of work or name

English

0 references

publication date

1 June 1998

1 reference

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American Journal of Human Genetics

11 November 2019

published in

1 reference

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11 November 2019

volume

62

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11 November 2019

issue

6

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11 November 2019

page(s)

1493-1499

1 reference

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Paternal Transmission of X-Linked Placental Dysplasia in Mouse Interspecific Hybrids

11 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Epistatic control of non-Mendelian inheritance in mouse interspecific crosses

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Segregation distortion of the CTG repeats at the myotonic dystrophy 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=1377139

Heritability of X chromosome--inactivation phenotype in a large family

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrid

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

The genetics of retinoblastoma, revisited

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Escape from X inactivation in human and mouse

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377139

A 2D crossover-based map of the human X chromosome as a model for map integration

27 October 2018

1 reference

12 December 2020

Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation

1 reference

12 December 2020

Non-mendelian inheritance of X chromosome markers in interspecific backcrosses

1 reference

12 December 2020

Encyclopedia of the mouse genome V. Mouse X chromosome

1 reference

12 December 2020

Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22

1 reference

12 December 2020

Segregation distortion of X-linked marker genes in interspecific crosses between Mus musculus and M. spretus

1 reference

12 December 2020

Identifiers

DOI

10.1086/301860

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9585588%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9585588%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

PubMed publication ID

9585588

1 reference