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

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About: A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) հոդված (hy) wetenschappelijk artikel (nl) наукова стаття, опублікована в 1994 (uk) im Januar 1994 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57339580-9396B3D6-4C58-4066-9181-94155DB24A95 wds:Q57339580-FBFCF158-B366-40B7-9891-28B0943B57AF
publication date	1994-01-01 00:00:00Z (xsd:dateTime) 1994-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57339580-DA8D22D9-6A89-4B90-B328-B006FC51840E
language of work or name	English
author name string	wds:Q57339580-0001F36C-FCCE-4FA1-B4E3-87B5A751DF76 wds:Q57339580-0F8A9F2E-26D1-4145-8CCC-2C0980E86CED wds:Q57339580-4B33525E-AD03-4A97-BEC5-1E8C02D02377 wds:Q57339580-6F149EBB-2DD2-4CD1-9F0C-BB45C17393DE wds:Q57339580-8658D977-40A4-4BA5-81C6-67F8B1C0375D wds:Q57339580-8DF72280-8C7E-4572-8349-0270239C63DB wds:Q57339580-9F59DD3A-7793-466A-9ADD-9CE1BF5501C7 wds:Q57339580-ACA14DC3-0088-4385-9D49-25F36ECD6CEB wds:Q57339580-B36FD15C-0EA5-48A5-B2E7-ACD4DF1DD53D wds:Q57339580-C901F3E4-6BC1-42F1-A9FB-768C59C31DA6 wds:Q57339580-E81B08CB-1821-4BE4-995C-7DA7B714D21D wds:Q57339580-FC3C8FB3-B374-443B-9ADA-7A15A49D021D
author name string	Jacqueline Levilliers Hassan Chaib C Petit J Levilliers P Guilford Geneviéve Lina-Granade Henri Plauchu H Plauchu A Morgon G Lina-Granade H Chaïb Alain Morgon
rdfs:label	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (en) A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (nl)
skos:prefLabel	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (en) A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (nl)
name	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (en) A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (nl)
author	wds:Q57339580-32B10C57-B0A0-4657-9837-99D1402BC17E wds:Q57339580-EF1815F4-DBD8-4CF0-B129-AA452531ED34
author	Christine Petit Parry Guilford
title	wds:Q57339580-4848AB5F-0994-4DCF-88DA-846F94BCE890
title	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval (en)
page(s)	wds:Q57339580-59640D27-D94A-47D3-ABA2-9F8C3FFB9C7A wds:Q57339580-99D958DF-BE0F-46FF-99BC-0757328CC583
page(s)	2219-2222 2219-22
instance of	wds:Q57339580-ECAACB06-4584-43D4-AC7B-DB08D61490F2
instance of	scholarly article
main subject	wds:Q57339580-B123C37D-E79E-4D38-9CF0-915009FD97FF
main subject	deafness
PubMed ID	wds:Q57339580-554C66FF-4499-46C6-BA96-A5E18187D42F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7881423
PubMed ID	7881423
published in	wds:Q57339580-2ED7A395-B598-41CA-8689-91A79CBDE6DC
published in	Human Molecular Genetics
issue	wds:Q57339580-5E3581FF-D0C5-4AA3-8A1E-8CD4D6FFEC69
volume	wds:Q57339580-7A5C797C-3405-416C-B9C8-4CB16817E6D7
issue	12
volume	3
DOI	wds:Q57339580-20F73759-39A5-4C0C-89D9-CB430D3459AA
DOI	http://dx.doi.org/10.1093/HMG/3.12.2219
DOI	10.1093/HMG/3.12.2219
is owl:sameAs of	A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57339580
is cites work of	Non-syndromic autosomal-dominant deafness Connexin 26 mutations in hereditary non-syndromic sensorineural deafness Genes responsible for human hereditary deafness: symphony of a thousand Connexin 26 gene linked to a dominant deafness. A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22-23 An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. Linkage analysis in Usher syndrome type I (USH1) families from Spain Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes Autosomal recessive nonsyndromic hearing loss A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24 Genetics of deafness A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3. GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss loci Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175. Functional analysis of human Cx26 mutations associated with deafness Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes Sensorineural hearing loss in children Gap junctions in inherited human disease The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region Beginning of a molecular era in hearing and deafness Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder Did the GJB2 35delG mutation originate in Iran? Genetic hearing loss. Past and future. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p

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