Authors:
Bykhovskaya, Y
Yang, HY
Taylor, K
Hang, T
Tun, RYM
Estivill, X
Casano, RAMS
Majamaa, K
Shohat, M
Fischel-Ghodsian, N
Citation: Y. Bykhovskaya et al., Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness, GENET MED, 3(3), 2001, pp. 177-180
Authors:
Spirina, O
Bykhovskaya, Y
Kajava, AV
O'Brien, TW
Nierlich, DP
Mougey, EB
Sylvester, JE
Graack, HR
Wittmann-Liebold, B
Fischel-Ghodsian, N
Citation: O. Spirina et al., Heart-specific splice-variant of a human mitochondrial ribosomal protein (mRNA processing; tissue specific splicing), GENE, 261(2), 2000, pp. 229-234
Authors:
Chen, XG
Bykhovskaya, Y
Tidow, N
Hamon, M
Bercovitz, Z
Spirina, O
Fischel-Ghodsian, N
Citation: Xg. Chen et al., The Familial Mediterranean Fever protein interacts and colocalizes with a putative Golgi transporter, P SOC EXP M, 224(1), 2000, pp. 32-40
Authors:
Bykhovskaya, Y
Estivill, X
Taylor, K
Hang, T
Hamon, M
Casano, RAMS
Yang, HY
Rotter, JI
Shohat, M
Fischel-Ghodsian, N
Citation: Y. Bykhovskaya et al., Candidate locus for a nuclear modifier gene for maternally inherited deafness, AM J HU GEN, 66(6), 2000, pp. 1905-1910
Authors:
Casano, RAMS
Johnson, DF
Bykhovskaya, Y
Torricelli, F
Bigozzi, M
Fischel-Ghodsian, N
Citation: Rams. Casano et al., Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications, AM J OTOLAR, 20(3), 1999, pp. 151-156
Authors:
Friedman, RA
Bykhovskaya, Y
Sue, CM
DiMauro, S
Bradley, R
Fallis-Cunningham, R
Paradies, N
Pensak, ML
Smith, RJ
Groden, J
Li, XYC
Fischel-Ghodsian, N
Citation: Ra. Friedman et al., Maternally inherited nonsyndromic hearing loss, AM J MED G, 84(4), 1999, pp. 369-372