Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness von Bykhovskaya, Yelena, Yang, Huiying, Taylor, Kent, Hang, Tieu, Tun, Richard Y M, Estivill, Xavier, Casano, Rosaria A M S, Majamaa, Kari, Shohat, Mordechai, Fischel-Ghodsian, Nathan

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Candidate Locus for a Nuclear Modifier Gene for Maternally Inherited Deafness von Bykhovskaya, Yelena, Estivill, Xavier, Taylor, Kent, Hang, Tieu, Hamon, Melanie, Casano, Rosaria A.M.S., Yang, Huiying, Rotter, Jerome I., Shohat, Mordechai, Fischel-Ghodsian, Nathan

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Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications von Casano, Rosaria A.M.S., Johnson, David F., Bykhovskaya, Yelena, Torricelli, Francesca, Bigozzi, Minna, Fischel-Ghodsian, Nathan

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Intracellular calcium accumulation and responsiveness to progesterone in capacitating human spermatozoa von Baldi, E, Casano, R, Falsetti, C, Krausz, C, Maggi, M, Forti, G

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Hearing loss due to the mitochondrial A1555G mutation in Italian families von Casano, Rosaria A.M.S., Bykhovskaya, Yelena, Johnson, David F., Hamon, Melanie, Torricelli, Francesca, Bigozzi, Minna, Fischel-Ghodsian, Nathan

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Decreased responsiveness to progesterone of spermatozoa in oligozoospermic patients von Falsetti, C, Baldi, E, Krausz, C, Casano, R, Failli, P, Forti, G

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Simultaneous measurement of seminal L-carnitine, α,1-4-glucosidase, and glycerylphosphorylcholine in azoospermic and Oligozoospermic patients von Casano, Rosaria, Orlando, Claudio, Caldini, Anna L., Barni, Tullio, Natali, Alessandro, Serio, Mario

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Measurement of seminal LDH-X and transferrin in normal and infertile men von Orlando, C, Casano, R, Caldini, A. L, Forti, G, Barni, T, Bonfanti, L, Serio, M

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