1. Anirdia‐like phenotype caused by 6p25 dosage aberrations. (March 2015) Authors: Arcot Sadagopan, Karthikeyan; Liu, Grace T.; Capasso, Jenina E.; Wuthisiri, Wadakarn; Keep, Rosanne B.; Levin, Alex V. Journal: American journal of medical genetics Issue: Volume 167:Number 3(2015:Mar.) Page Start: 524 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son. (June 2015) Authors: Arcot Sadagopan, Karthikeyan; Battista, Robert; Keep, Rosanne B.; Capasso, Jenina E.; Levin, Alex V. Journal: Ophthalmic genetics Issue: Volume 36:Number 2(2015:Jun.) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cutaneous freckling: Possible new clinical marker for the diagnosis of Hermansky-Pudlak syndrome in Indian Asian patients with oculocutaneous albinism. (4th March 2017) Authors: Arcot Sadagopan, Karthikeyan; Kathirvel, Renugadevi; Keep, Rosanne B.; Sundaresan, P.; Huang, Hui; Rolfs, Arndt; Parthiban, Kannan; Vijayalakshmi, P. Journal: Ophthalmic genetics Issue: Volume 38:Number 2(2017) Page Start: 194 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗