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G Bademci

Showing results (21-30 of 24) with videos related to

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Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.
Clinical Genetics|September 9, 2015
A Mayan founder mutation is a common cause of deafness in GuatemalaC Carranza, I Menendez, M Herrera, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 11, 2022
Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing lossB Vona, D A Schwartzbaum, A A Rodriguez, et al.
Scientific Reports|August 27, 2016
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossG Bademci, F B Cengiz, J Foster Ii, et al.
Pageof 3

Showing results (21-30 of 24) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 24 results.
Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.
Clinical Genetics|September 9, 2015
A Mayan founder mutation is a common cause of deafness in GuatemalaC Carranza, I Menendez, M Herrera, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 11, 2022
Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing lossB Vona, D A Schwartzbaum, A A Rodriguez, et al.
Scientific Reports|August 27, 2016
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing LossG Bademci, F B Cengiz, J Foster Ii, et al.
Pageof 3