(Q70659381)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

4

Rotter JI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

Bu X

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Shohat M

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

Jaber L

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

publication date

1 January 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

3-15

1 reference

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A new look at the statistical model identification

13 October 2019

cites work

1 reference

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7 January 2021

Relaxed Cellular Controls and Organelle Heredity

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

On the statistical determination of major gene mechanisms in continuous human traits: regressive models.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Regressive logistic models for familial disease and other binary traits

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Two-locus mitochondrial and nuclear gene models for mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Probability functions on complex pedigrees

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

The generation of transplasmic Drosophila simulans by cytoplasmic injection: effects of segregation and selection on the perpetuation of mitochondrial DNA heteroplasmy.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Maternal inheritance of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Variable genotype of Leber's hereditary optic neuropathy patients.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Segregation analysis in human genetics

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Complete replacement of mitochondrial DNA in Drosophila

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

On some models for segregation analysist?

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Biochemical characterization of a pedigree with mitochondrially inherited deafness

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.1370100102

7 January 2021

Identifiers

DOI

10.1002/GEPI.1370100102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8472932%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference