Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175. (Q50516919)

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scientific article published in January 1996

Language	Label	Description	Also known as
English	Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.	scientific article published in January 1996

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

author name string

K A Brown

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

A H Janjua

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

G Karbani

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

G Parry

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

A Noble

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

G Crockford

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

V E Newton

8

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

A F Markham

9

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

R F Mueller

10

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

publication date

1 January 1996

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

Human Molecular Genetics

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

169-173

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

Epidemiology of hearing loss and aetiological diagnosis of hearing impairment in childhood

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Aetiological diagnosis in hearing-impaired children--clinical value and application of a modern examination programme

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Genetic epidemiology of hearing impairment

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Traces of her workings

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Genes and deafness

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Estimated number of loci for autosomal recessive severe nerve deafness within the Israeli Jewish population, with implications for genetic counseling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

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

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

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

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

The gene for an inherited form of deafness maps to chromosome 5q31

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F5.1.169

21 January 2018

Identifiers

10.1093/HMG/5.1.169

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/8789457

ResearchGate publication ID

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