Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan (Q50516927)

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scientific article published in January 1996

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Language	Label	Description	Also known as
English	Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan	scientific article published in January 1996

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

title

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

main subject

Pakistan

1 reference

based on heuristic

inferred from title

deafness

1 reference

based on heuristic

inferred from title

author name string

Veske A

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

Oehlmann R

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

Younus F

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

Mohyuddin A

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

Müller-Myhsok B

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

Mehdi SQ

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

Gal A

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

publication date

1 January 1996

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

published in

Human Molecular Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

volume

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

page(s)

165-168

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

cites work

Genes and deafness

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.165

retrieved

21 January 2018

Identifiers

DOI

10.1093/HMG/5.1.165

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

PubMed publication ID

8789456

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8789456

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/8789456

ResearchGate publication ID

14414478

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