(Q50481505)

English

Two patients with severe corneal disease in KID syndrome.

scientific article published in January 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Two patients with severe corneal disease in KID syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

corneal disease

1 reference

based on heuristic

inferred from title

author name string

Shozo Sonoda

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Eisuke Uchino

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Koh-Hei Sonoda

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Shinichi Yotsumoto

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Eiichi Uchio

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Yasushi Isashiki

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

Taiji Sakamoto

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

language of work or name

0 references

publication date

1 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

American Journal of Ophthalmology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

137

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

181-183

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

The Keratitis, Ichthyosis, and Deafness (KID) Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2803%2900739-6

7 January 2021

Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2803%2900739-6

7 January 2021

Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2803%2900739-6

7 January 2021

Genetic diseases and gene knockouts reveal diverse connexin functions.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2803%2900739-6

7 January 2021

Keratitis, ichthyosis, and deafness (KID syndrome): review of the literature and proposal of a new terminology

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2803%2900739-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0002-9394(03)00739-6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/14700667

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