(Q50516927)

14 March 2018

title

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

1 reference

14 March 2018

1 reference

1 reference

Veske A

1

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14 March 2018

Oehlmann R

2

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14 March 2018

Younus F

3

1 reference

14 March 2018

Mohyuddin A

4

1 reference

14 March 2018

Müller-Myhsok B

5

1 reference

14 March 2018

Mehdi SQ

6

1 reference

14 March 2018

Gal A

7

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14 March 2018

publication date

1 January 1996

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14 March 2018

published in

Human Molecular Genetics

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14 March 2018

volume

5

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14 March 2018

issue

1

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14 March 2018

page(s)

165-168

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14 March 2018

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

1 reference

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

21 January 2018

Identifiers

DOI

10.1093/HMG/5.1.165

1 reference

14 March 2018

PubMed ID

8789456

1 reference

14 March 2018