Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics.

Por Fischel-Ghodsian, N
Publicado em 1998

Long range genome structure around the human alpha-globin complex analysed by PFGE.

Por Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
Publicado em 1987

Unusual features of CpG-rich (HTF) islands in the human alpha globin complex: association with non-functional pseudogenes and presence within the 3' portion of the zeta gene.

Por Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
Publicado em 1987

Rapid detection of the hemoglobin C mutation by allele-specific polymerase chain reaction.

Por Fischel-Ghodsian, N, Hirsch, P C, Bohlman, M C
Publicado em 1990

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Por Shohat, M, Lotan, R, Magal, N, Shohat, T, Fischel-Ghodsian, N, Rotter, J I, Jaber, L
Publicado em 1997

A molecular basis for human hypersensitivity to aminoglycoside antibiotics.

Por Hutchin, T, Haworth, I, Higashi, K, Fischel-Ghodsian, N, Stoneking, M, Saha, N, Arnos, C, Cortopassi, G
Publicado em 1993

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

Por Pandya, A, Xia, X, Radnaabazar, J, Batsuuri, J, Dangaansuren, B, Fischel-Ghodsian, N, Nance, W E
Publicado em 1997

Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple non-parametric analyses

Por Yang, H, Plevy, S, Taylor, K, Tyan, D, Fischel-Ghodsian, N, McElree, C, Targan, S, Rotter, J
Publicado em 1999

Sensorineural deafness inherited as a tissue specific mitochondrial disorder.

Por Jaber, L, Shohat, M, Bu, X, Fischel-Ghodsian, N, Yang, H Y, Wang, S J, Rotter, J I
Publicado em 1992

Candidate locus for a nuclear modifier gene for maternally inherited deafness.

Por Bykhovskaya, Y, Estivill, X, Taylor, K, Hang, T, Hamon, M, Casano, R A, Yang, H, Rotter, J I, Shohat, M, Fischel-Ghodsian, N
Publicado em 2000

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity.

Por Shohat, M, Bu, X, Shohat, T, Fischel-Ghodsian, N, Magal, N, Nakamura, Y, Schwabe, A D, Schlezinger, M, Danon, Y, Rotter, J I
Publicado em 1992

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

Por Wilkie, A O, Zeitlin, H C, Lindenbaum, R H, Buckle, V J, Fischel-Ghodsian, N, Chui, D H, Gardner-Medwin, D, MacGillivray, M H, Weatherall, D J, Higgs, D R
Publicado em 1990

Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

Por Levy, E. N., Shen, Y., Kupelian, A., Kruglyak, L., Aksentijevich, I., Pras, E., Balow, J. E., Linzer, B., Chen, X., Shelton, D. A., Gumucio, D., Pras, M., Shohat, M., Rotter, J. I., Fischel-Ghodsian, N., Richards, R. I., Kastner, D. L.
Publicado em 1996