Corneal dystrophy-perceptive deafness syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Corneal dystrophy-perceptive deafness syndrome" in English language version.

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arizona.edu

disorders.eyes.arizona.edu

"corneal dystrophy and sensorineural deafness | Hereditary Ocular Diseases". disorders.eyes.arizona.edu. Retrieved 2022-08-03.

doi.org

Desir, Julie; Moya, Graciela; Reish, Orit; Van Regemorter, Nicole; Deconinck, Hilde; David, Karen L.; Meire, Françoise M.; Abramowicz, Marc J. (2007-05-01). "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy". Journal of Medical Genetics. 44 (5): 322–326. doi:10.1136/jmg.2006.046904. ISSN 1468-6244. PMC 2597979. PMID 17220209.

eugenelabs.com

"Helpful information about | Eugene Australia". eugenelabs.com. Archived from the original on 2022-08-03. Retrieved 2022-08-03.

nih.gov

rarediseases.info.nih.gov

"Corneal dystrophy and perceptive deafness - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2022-08-03. Retrieved 2022-08-03.

ncbi.nlm.nih.gov

Desir, Julie; Moya, Graciela; Reish, Orit; Van Regemorter, Nicole; Deconinck, Hilde; David, Karen L.; Meire, Françoise M.; Abramowicz, Marc J. (2007-05-01). "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy". Journal of Medical Genetics. 44 (5): 322–326. doi:10.1136/jmg.2006.046904. ISSN 1468-6244. PMC 2597979. PMID 17220209.

pubmed.ncbi.nlm.nih.gov

Desir, Julie; Moya, Graciela; Reish, Orit; Van Regemorter, Nicole; Deconinck, Hilde; David, Karen L.; Meire, Françoise M.; Abramowicz, Marc J. (2007-05-01). "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy". Journal of Medical Genetics. 44 (5): 322–326. doi:10.1136/jmg.2006.046904. ISSN 1468-6244. PMC 2597979. PMID 17220209.

omim.org

"Entry - #217400 - CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS; CDPD - OMIM". www.omim.org. Retrieved 2022-08-03.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Corneal dystrophy perceptive deafness syndrome". www.orpha.net. Retrieved 2022-08-03.{{cite web}}: CS1 maint: numeric names: authors list (link)

rarediseases.org

"Corneal dystrophy and perceptive deafness".

sema4.com

"Corneal Dystrophy and Perceptive Deafness (SLC4A11)". Sema4. 2017-02-01. Retrieved 2022-08-03.

web.archive.org

"Corneal dystrophy and perceptive deafness - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2022-08-03. Retrieved 2022-08-03.
"Helpful information about | Eugene Australia". eugenelabs.com. Archived from the original on 2022-08-03. Retrieved 2022-08-03.

webmd.com

Newman, Dennis. "Corneal Dystrophies: Symptoms, Causes, and Treatment". WebMD. Retrieved 2022-08-03.

worldcat.org

Desir, Julie; Moya, Graciela; Reish, Orit; Van Regemorter, Nicole; Deconinck, Hilde; David, Karen L.; Meire, Françoise M.; Abramowicz, Marc J. (2007-05-01). "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy". Journal of Medical Genetics. 44 (5): 322–326. doi:10.1136/jmg.2006.046904. ISSN 1468-6244. PMC 2597979. PMID 17220209.