(Q50485173)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

title

A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

author name string

A R Parrado

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

publication date

1 January 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

volume

63

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

page(s)

39-45

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

Murine acid alpha-glucosidase: cell-specific mRNA differential expression during development and maturation

16 December 2019

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.630106.X

Two deaf mice, two deaf mice...

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Comprehensive human genetic maps: individual and sex-specific variation in recombination

1 reference

12 December 2020

At the speed of sound: gene discovery in the auditory system

1 reference

12 December 2020

Computer programs for multilocus haplotyping of general pedigrees.

1 reference

12 December 2020

Improved set of short-tandem-repeat polymorphisms for screening the human genome.

1 reference

12 December 2020

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

1 reference

12 December 2020

Faster sequential genetic linkage computations

1 reference

12 December 2020

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

1 reference

12 December 2020

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

12 December 2020

Nonsyndromic hearing impairment: unparalleled heterogeneity

1 reference

12 December 2020

A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.

1 reference

12 December 2020

A high-resolution recombination map of the human genome

1 reference

12 December 2020

A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.

1 reference

12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1034/J.1399-0004.2003.630106.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12519370%20AND%20SRC:MED&resulttype=core&format=json

16 December 2019

PubMed publication ID

12519370

1 reference