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Rosanne B Keep

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Ophthalmic Genetics|October 8, 2013
Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and SonKarthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Anirdia-like phenotype caused by 6p25 dosage aberrationsKarthikeyan Arcot Sadagopan, Grace T Liu, Jenina E Capasso, et al.
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Showing results (1-10 of 2) with videos related to

Sort By:
Pageof 1
Ophthalmic Genetics|October 8, 2013
Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and SonKarthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, et al.
American Journal of Medical Genetics. Part A|February 19, 2015
Anirdia-like phenotype caused by 6p25 dosage aberrationsKarthikeyan Arcot Sadagopan, Grace T Liu, Jenina E Capasso, et al.
Pageof 1