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M A Musarella

Showing results (21-30 of 43) with videos related to

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Journal of Pediatric Ophthalmology and Strabismus|March 1, 1982
Oculomotor abnormalities in chronic GM2 gangliosidosisM A Musarella, E L Raab, S H Rudolph, et al.
Human Mutation|January 1, 1992
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosisO Riess, B Weber, A Noeremolle, et al.
Genomics|April 1, 1991
Linkage analysis in X-linked ocular albinismR E Schnur, R L Nussbaum, L Anson-Cartwright, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1992
Peters' anomaly. The spectrum of associated ocular and systemic malformationsE Heon, M Barsoum-Homsy, L Cevrette, et al.
Genomics|May 1, 1989
Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrierM A Musarella, L Anson-Cartwright, A Burghes, et al.
American Journal of Human Genetics|October 1, 1988
Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysisM A Musarella, A Burghes, L Anson-Cartwright, et al.
American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
Genomics|October 1, 1990
Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa familiesM A Musarella, L Anson-Cartwright, S M Leal, et al.
Genomics|October 1, 1991
Physical mapping at a potential X-linked retinitis pigmentosa locus (RP3) by pulsed-field gel electrophoresisM A Musarella, C L Anson-Cartwright, C McDowell, et al.
Human Mutation|January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)R A Spritz, S T Lee, K Fukai, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Journal of Pediatric Ophthalmology and Strabismus|March 1, 1982
Oculomotor abnormalities in chronic GM2 gangliosidosisM A Musarella, E L Raab, S H Rudolph, et al.
Human Mutation|January 1, 1992
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosisO Riess, B Weber, A Noeremolle, et al.
Genomics|April 1, 1991
Linkage analysis in X-linked ocular albinismR E Schnur, R L Nussbaum, L Anson-Cartwright, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1992
Peters' anomaly. The spectrum of associated ocular and systemic malformationsE Heon, M Barsoum-Homsy, L Cevrette, et al.
Genomics|May 1, 1989
Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrierM A Musarella, L Anson-Cartwright, A Burghes, et al.
American Journal of Human Genetics|October 1, 1988
Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysisM A Musarella, A Burghes, L Anson-Cartwright, et al.
American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
Genomics|October 1, 1990
Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa familiesM A Musarella, L Anson-Cartwright, S M Leal, et al.
Genomics|October 1, 1991
Physical mapping at a potential X-linked retinitis pigmentosa locus (RP3) by pulsed-field gel electrophoresisM A Musarella, C L Anson-Cartwright, C McDowell, et al.
Human Mutation|January 1, 1997
Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)R A Spritz, S T Lee, K Fukai, et al.
Pageof 5