(Q28290197)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

0 references

1 reference

1 reference

D A Scott

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

R Carmi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

K Elbedour

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

G M Duyk

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

E M Stone

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

V C Sheffield

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

language of work or name

English

0 references

publication date

1 October 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

21 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

965-968

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

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

21 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

A microsatellite genetic linkage map of human chromosome 13.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

Integrated human genome-wide maps constructed using the CEPH reference panel.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801487

[Congenital sensorineural deafness and associated syndromes]

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7573061

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7573061

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7573061

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7573061%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

PubMed publication ID

7573061

1 reference