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Long range genome structure around the human α-globin complex analysed by PFGEFISCHEL-GHODSIAN, N; NICHOLLS, R. D; HIGGS, D. R et al.Nucleic acids research. 1987, Vol 15, Num 15, pp 6197-6207, issn 0305-1048Article

Recombination at the human α-globin gene cluster: sequence features and topological constraintsNICHOLLS, R. D; FISCHEL-GHODSIAN, N; HIGGS, D. R et al.Cell (Cambridge). 1987, Vol 49, Num 3, pp 369-378, issn 0092-8674Article

Corrections to the human mitochondrial ribosomal RNA sequencesPREZANT, T. R; AGAPIAN, J. V; FISCHEL-GHODSIAN, N et al.Human genetics. 1994, Vol 93, Num 1, pp 87-88, issn 0340-6717Article

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555GSHOHAT, M; FISCHEL-GHODSIAN, N; LEGUM, C et al.American journal of otolaryngology. 1999, Vol 20, Num 1, pp 64-67, issn 0196-0709Article

Unusual features of CpG-rich (HTF) islands in the human α globin complex: association with non-functional pseudogenes and presence within the 3' portion of the ζ geneFISCHEL-GHODSIAN, N; NICHOLLS, R. D; HIGGS, D. R et al.Nucleic acids research. 1987, Vol 15, Num 22, pp 9215-9225, issn 0305-1048Article

Isolation of overexpressed yeast genes which prevent aminoglycoside toxicityJOHNSON, D. F; PREZANT, T. R; LUBAVIN, B et al.Hearing research. 1998, Vol 120, Num 1-2, pp 62-68, issn 0378-5955Article

Mitochondrial mutation associated with nonsyndromic deafnessFISCHEL-GHODSIAN, N; PREZANT, T. R; FOURNIER, P et al.American journal of otolaryngology. 1995, Vol 16, Num 6, pp 403-408, issn 0196-0709Article

Arthrogryposis multiplex congenita in an Arab kindred : updateJABER, L; WEITZ, R; XIANGDONG BU et al.American journal of medical genetics. 1995, Vol 55, Num 3, pp 331-334, issn 0148-7299Article

Biochemical characterization of a pedigree with mitochondrially inherited deafnessPREZANT, T. R; SHOHAT, M; JABER, L et al.American journal of medical genetics. 1992, Vol 44, Num 4, pp 465-472, issn 0148-7299Article

Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple non-parametric analysesYANG, H; PLEVY, S. E; TAYLOR, K et al.Gut. 1999, Vol 44, Num 4, pp 519-526, issn 0017-5749Article

Identification of two Krüppel-related zinc finger genes (ZNF200 and ZNF210) from human chromosome 16p13.3ZUOMING DENG; CENTOLA, M; XIAOGUANG CHEN et al.Genomics (San Diego, Calif.). 1998, Vol 53, Num 1, pp 97-103, issn 0888-7543Article

An analysis of a large postlingually deaf family with hereditary non-syndromic profound hearing lossANGELI, S. I; NARANJO, C; FRIEDMAN, R. A et al.Acta oto-laryngologica. 1999, Vol 119, Num 2, pp 158-162, issn 0001-6489Conference Paper

mt-Nd2 allele of the ALR/Lt mouse confers resistance against both chemically induced and autoimmune diabetesMATHEWS, C. E; LEITER, E. H; SPIRINA, O et al.Diabetologia (Berlin). 2005, Vol 48, Num 2, pp 261-267, issn 0012-186X, 7 p.Article

Temporal bone histopathology in Connexin 26-related hearing lossJUN, A. I; MCGUIRT, W. T; HINOJOSA, R et al.The Laryngoscope. 2000, Vol 110, Num 2, pp 269-275, issn 0023-852X, 1Article

Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafnessSEVIOR, K. B; HATAMOCHI, A; STEWART, I. A et al.American journal of medical genetics. 1998, Vol 75, Num 2, pp 179-185, issn 0148-7299Article

Screening for mtDNA diabetes mutations in Pima Indians with NIDDMSEPEHRNIA, B; PREZANT, T. R; ROTTER, J. I et al.American journal of medical genetics. 1995, Vol 56, Num 2, pp 198-202, issn 0148-7299Article

A molecular basis for human hypersensitivity to aminoglycoside antibioticsHUTCHIN, T; HAWORTH, I; HIGASHI, K et al.Nucleic acids research. 1993, Vol 21, Num 18, pp 4174-4179, issn 0305-1048Article

Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeFISCHEL-GHODSIAN, N; BOHLMAN, C; PREZANT, T. R et al.Pediatric research. 1992, Vol 31, Num 6, pp 557-560, issn 0031-3998Article

Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA^Ser(UCN) geneSUE, C. M; TANJI, K; FISCHEL-GHODSIAN, N et al.Neurology. 1999, Vol 52, Num 9, pp 1905-1908, issn 0028-3878Article

Mosaic trisomy 16 ascertained through amniocentesis : Evaluation of 11 new casesHSU, W.-T; SHCHEPIN, D. A; HAJIANPOUR, M. J et al.American journal of medical genetics. 1998, Vol 80, Num 5, pp 473-480, issn 0148-7299Article

Maternally inherited nonsyndromic hearing lossFRIEDMAN, R. A; BYKHOVSKAYA, Y; LI, X. C et al.American journal of medical genetics. 1999, Vol 84, Num 4, pp 369-372, issn 0148-7299Article

A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsBALOW, J. E; SHELTON, D. A; LEVY, E. N et al.Genomics (San Diego, Calif.). 1997, Vol 44, Num 3, pp 280-291, issn 0888-7543Article

Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitisOHMEN, J. D; YANG, H.-Y; TARGAN, S et al.Human molecular genetics (Print). 1996, Vol 5, Num 10, pp 1679-1683, issn 0964-6906Article

Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4DE KOK, Y. J. M; VOSSENAAR, E. R; THORPE, P et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1229-1235, issn 0964-6906Article