Search research articles
Contact Us
Filters
Showing results (1-10 of 4) with videos related to
Page
of 1
Sort By:
Clinical & Experimental Ophthalmology
|
July 24, 2010
Identification of a novel deletion in the OA1 gene: report of the first Spanish family with X-linked ocular albinism
Monica Martinez-Garcia, Rosa Riveiro-Alvarez, Cristina Villaverde-Montero, et al.
Investigative Ophthalmology & Visual Science
|
December 5, 2009
Comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning in the ABCA4 gene
Jana Aguirre-Lamban, Rosa Riveiro-Alvarez, Maria Garcia-Hoyos, et al.
Investigative Ophthalmology & Visual Science
|
February 19, 2011
Further associations between mutations and polymorphisms in the ABCA4 gene: clinical implication of allelic variants and their role as protector/risk factors
Jana Aguirre-Lamban, Juan José González-Aguilera, Rosa Riveiro-Alvarez, et al.
Molecular Vision
|
March 28, 2020
Exome sequencing identifies <i>PEX6</i> mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment
Gema García-García, Iker Sanchez-Navarro, Elena Aller, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Clinical & Experimental Ophthalmology
|
July 24, 2010
Identification of a novel deletion in the OA1 gene: report of the first Spanish family with X-linked ocular albinism
Monica Martinez-Garcia, Rosa Riveiro-Alvarez, Cristina Villaverde-Montero, et al.
Investigative Ophthalmology & Visual Science
|
December 5, 2009
Comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning in the ABCA4 gene
Jana Aguirre-Lamban, Rosa Riveiro-Alvarez, Maria Garcia-Hoyos, et al.
Investigative Ophthalmology & Visual Science
|
February 19, 2011
Further associations between mutations and polymorphisms in the ABCA4 gene: clinical implication of allelic variants and their role as protector/risk factors
Jana Aguirre-Lamban, Juan José González-Aguilera, Rosa Riveiro-Alvarez, et al.
Molecular Vision
|
March 28, 2020
Exome sequencing identifies <i>PEX6</i> mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment
Gema García-García, Iker Sanchez-Navarro, Elena Aller, et al.
Page
of 1