(Q35631816)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21937999%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13 (English)

1 reference

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13 February 2020

1 reference

2

1 reference

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13 February 2020

Kwanghyuk Lee

3

1 reference

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13 February 2020

Sulman Basit

6

1 reference

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13 February 2020

8

Wasim Ahmad

1 reference

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13 February 2020

9

Suzanne M Leal

1 reference

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13 February 2020

author name string

Muhammad Ansar

1

1 reference

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13 February 2020

Syed Kamran-Ul-Hassan Naqvi

4

1 reference

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13 February 2020

Paula B Andrade

5

1 reference

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13 February 2020

Regie Lyn P Santos-Cortez

7

1 reference

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13 February 2020

publication date

22 September 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21937999%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

13 February 2020

published in

1 reference

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13 February 2020

volume

56

1 reference

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13 February 2020

issue

12

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13 February 2020

page(s)

866-868

1 reference

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A second-generation combined linkage physical map of the human genome

13 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Salt wasting and deafness resulting from mutations in two chloride channels

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Allegro, a new computer program for multipoint linkage analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Faster sequential genetic linkage computations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245365

12 July 2018

Identifiers

DOI

10.1038/JHG.2011.110

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21937999%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21937999%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

PubMed publication ID

21937999

1 reference