Francisco J Del Castillo - JoVE Visualize

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Investigative Ophthalmology & Visual Science|October 25, 2014

Contribution of mutation load to the intrafamilial genetic heterogeneity in a large cohort of Spanish retinal dystrophies familiesRocío Sánchez-Alcudia, Marta Cortón, Almudena Ávila-Fernández, et al.

American Journal of Human Genetics|November 6, 2012

Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairmentMargit Schraders, Laura Ruiz-Palmero, Ersan Kalay, et al.

American Journal of Human Genetics|October 23, 2003

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyIgnacio Del Castillo, Miguel A Moreno-Pelayo, Francisco J Del Castillo, et al.

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Showing results (21-30 of 23) with videos related to

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You have reached the last page of results.This site can display upto 23 results.

Investigative Ophthalmology & Visual Science|October 25, 2014

Contribution of mutation load to the intrafamilial genetic heterogeneity in a large cohort of Spanish retinal dystrophies familiesRocío Sánchez-Alcudia, Marta Cortón, Almudena Ávila-Fernández, et al.

American Journal of Human Genetics|November 6, 2012

Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairmentMargit Schraders, Laura Ruiz-Palmero, Ersan Kalay, et al.

American Journal of Human Genetics|October 23, 2003

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyIgnacio Del Castillo, Miguel A Moreno-Pelayo, Francisco J Del Castillo, et al.

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