Strategies for genetic study of hearing loss in the Brazilian northeastern region.

about

Targeted Resequencing of Deafness Genes Reveals a Founder MYO15A Variant in Northeastern Brazil.Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort

P2860

Q42778032-4A74E10F-B145-462D-99E2-874021BB03D1 Q58803935-A2EBCC1A-B515-4E0B-8569-C1C757DA26EF

P2860

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

Item

http://www.wikidata.org/entity/Q41987718

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

2014年论文

@zh

2014年论文

@zh-cn

name

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

@en

type

Item

label

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

@en

prefLabel

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

@en

P1476

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

@en

P2093

Hannalice G Cavalcanti

http://www.w3.org/2001/XMLSchema#string

Marine Rd Rosa

http://www.w3.org/2001/XMLSchema#string

Silvana Santos

http://www.w3.org/2001/XMLSchema#string

Uirá S Melo

http://www.w3.org/2001/XMLSchema#string

Vitor G Dantas

http://www.w3.org/2001/XMLSchema#string

Wagner T Andrade

http://www.w3.org/2001/XMLSchema#string

P2860

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

Nonsyndromic hearing impairment: unparalleled heterogeneity

Inbreeding in Brazil

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

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

ALOHOMORA: a tool for linkage analysis using 10K SNP array data.

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.

Usher's syndrome--deafness and progressive blindness. Clinical cases, prevention, theory and literature survey.

P304

11-21

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Regina Celia Mingroni Netto

P577

2014-02-17T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

24596593

http://www.w3.org/2001/XMLSchema#string

P932

3939003

http://www.w3.org/2001/XMLSchema#string

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

about

P2860

P2860

Strategies for genetic study of hearing loss in the Brazilian northeastern region.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P50

P577

P698

P932

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P50

P577

P698

P932