(Q50479155)

English

Refinement of the locus for non-syndromic sensorineural deafness (DFN2).

scientific article published in April 2004

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Refinement of the locus for non-syndromic sensorineural deafness (DFN2). (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

1 reference

based on heuristic

inferred from title

author name string

Bin Cui

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Haibing Zhang

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Yongzhong Lu

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Wei Zhong

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Gang Pei

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Xiangyin Kong

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Landian Hu

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

publication date

1 April 2004

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Journal of Genetics

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

83

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

35-38

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

Identification of a hot spot for microdeletions in patients with X- linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high risk registry to find congenital deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies for multilocus linkage analysis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of DFN2 to Xq22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15240907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02715827

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/15240907

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50479155&oldid=2231778143"