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Shyana Harper
Shyana Harper
Harvard University
Biology
Anatomy
Genetics
Locus heterogeneity
Cohort
4
Papers
2
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Molecular characterization of SNRNP200 mutations causing autosomal dominant retinitis pigmentosa with incomplete penetrance and phenotypic variability
2014
Investigative Ophthalmology & Visual Science
Carlo Rivolta
Paola Benaglio
Tremeur Guillaumie
Gaël Manes
Shyana Harper
Eliot L. Berson
Isabelle Meunier
Christian P. Hamel
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Citations (1)
Mutation Screening Of The FAM161A Gene (RP28) In An Autosomal Recessive Retinitis Pigmentosa Cohort
2011
Investigative Ophthalmology & Visual Science
Silvio Alessandro Di Gioia
Giulia Venturini
Shyana Harper
Eliot L. Berson
Carlo Rivolta
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Next Generation Sequencing Of Pooled DNA From A Large Cohort Of Patients Reveals New SNRNP200 Mutations Associated With Retinitis Pigmentosa
2011
Investigative Ophthalmology & Visual Science
Paola Benaglio
Leonardo P. Capelli
Shyana Harper
Eliot L. Berson
Carlo Rivolta
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Does pretreating the central cornea prevent central islands before photo refractive keratectomy (PRK)
1997
Investigative Ophthalmology & Visual Science
Shyana Harper
Juan-Carlos Abad
Dimitri T. Azar
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