(Q50507810)

English

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

scientific article published in November 1997

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scholarly article

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. (English)

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

1 reference

based on heuristic

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author name string

M M Carrasquillo

1

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

J Zlotogora

2

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

S Barges

3

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

A Chakravarti

4

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

publication date

1 November 1997

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

Human Molecular Genetics

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

6

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

2163-2172

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

12

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

Genes responsible for human hereditary deafness: symphony of a thousand

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

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%2F6.12.2163

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%2F6.12.2163

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%2F6.12.2163

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%2F6.12.2163

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%2F6.12.2163

21 January 2018

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22-23

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.12.2163

21 January 2018

Identifiers

10.1093/HMG/6.12.2163

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

1 reference

Europe PubMed Central

14 March 2018

http://europepmc.org/abstract/MED/9328482

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