Síndrome de Tietz (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome de Tietz" in Spanish language version.

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archive.org

Tietz W (Sep 1963). «A Syndrome of Deaf-Mutism Associated with Albinism Showing Dominant Autosomal Inheritance» (Free full text). Am. J. Hum. Genet. 15 (3): 259-264. PMC 1932384. PMID 13985019.

bmj.com

jmg.bmj.com

Smith SD, Kelley PM, Kenyon JB, Hoover D (Jun 2000). «Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF» (Free full text). J. Med. Genet. 37 (6): 446-448. PMC 1734605. PMID 10851256. doi:10.1136/jmg.37.6.446.

doi.org

dx.doi.org

Smith SD, Kelley PM, Kenyon JB, Hoover D (Jun 2000). «Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF» (Free full text). J. Med. Genet. 37 (6): 446-448. PMC 1734605. PMID 10851256. doi:10.1136/jmg.37.6.446.
Amiel J, Watkin PM, Tassabehji M, Read AP, Winter RM (Jan 1998). «Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)». Clin. Dysmorphol. 7 (1): 17-20. PMID 9546825. doi:10.1097/00019605-199801000-00003.

nih.gov

ncbi.nlm.nih.gov

Smith SD, Kelley PM, Kenyon JB, Hoover D (Jun 2000). «Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF» (Free full text). J. Med. Genet. 37 (6): 446-448. PMC 1734605. PMID 10851256. doi:10.1136/jmg.37.6.446.
Amiel J, Watkin PM, Tassabehji M, Read AP, Winter RM (Jan 1998). «Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)». Clin. Dysmorphol. 7 (1): 17-20. PMID 9546825. doi:10.1097/00019605-199801000-00003.
Tietz W (Sep 1963). «A Syndrome of Deaf-Mutism Associated with Albinism Showing Dominant Autosomal Inheritance» (Free full text). Am. J. Hum. Genet. 15 (3): 259-264. PMC 1932384. PMID 13985019.

orpha.net

Orphanet: Síndrome de Tietz. Consultado el 3 de marzo de 2016