Publications by authors named "Rosanne Keep"

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Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism.
Karthikeyan Arcot Sadagopan, Renugadevi Kathirvel, Rosanne B Keep, P Sundaresan, Hui Huang

Ophthalmic Genet· November 2017

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Organophosphate retinopathy.
Hang Pham, Michelle D Lingao, Anuradha Ganesh, Jenina E Capasso, Rosanne Keep

Oman J Ophthalmol· March 2016

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Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son.
Karthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, Jenina E Capasso, Alex V Levin

Ophthalmic Genet· June 2015

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Anirdia-like phenotype caused by 6p25 dosage aberrations.
Karthikeyan Arcot Sadagopan, Grace T Liu, Jenina E Capasso, Wadakarn Wuthisiri, Rosanne B Keep

Am J Med Genet A· March 2015

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Genetic testing in retinal dystrophies.
Anuradha Ganesh, Rosanne B Keep

Oman J Ophthalmol· September 2011

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Population-based Tay-Sachs screening among Ashkenazi Jewish young adults in the 21st century: Hexosaminidase A enzyme assay is essential for accurate testing.
Adele Schneider, Sachiko Nakagawa, Rosanne Keep, Darnelle Dorsainville, Joel Charrow

Am J Med Genet A· November 2009

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Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughters.
Adele Schneider, Tanya M Bardakjian, Jie Zhou, Nkecha Hughes, Rosanne Keep

Am J Med Genet A· November 2008

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