Ben Othmane K - Search Results

1

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Ben Othmane K, et al. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

2

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.

Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Baxter RV, et al. Among authors: ben othmane k. Nat Genet. 2002 Jan;30(1):21-2. doi: 10.1038/ng796. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743579

3

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, et al. Ben Othmane K, et al. Nat Genet. 1992 Dec;2(4):315-7. doi: 10.1038/ng1292-315. Nat Genet. 1992. PMID: 1303286

4

Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, et al. Ben Othmane K, et al. Genomics. 1993 Aug;17(2):370-5. doi: 10.1006/geno.1993.1334. Genomics. 1993. PMID: 8406488

5

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.

Ben Othmane K, Rochelle JM, Ben Hamida M, Slotterbeck B, Rao N, Hentati F, Pericak-Vance MA, Vance JM. Ben Othmane K, et al. Neurogenetics. 1998 Dec;2(1):18-23. doi: 10.1007/s100480050047. Neurogenetics. 1998. PMID: 9933296

6

[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty].

Ben Hamida M, Ben Othmane K, Belal S, Hentati F. Ben Hamida M, et al. Among authors: ben othmane k. Rev Neurol (Paris). 1995 Apr;151(4):221-4. Rev Neurol (Paris). 1995. PMID: 7481371 Review. French. No abstract available.

7

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C).

Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, Loeb D, Hentati F, Roses AD, et al. Ben Othmane K, et al. Am J Hum Genet. 1995 Sep;57(3):732-4. Am J Hum Genet. 1995. PMID: 7668303 Free PMC article. No abstract available.

8

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.

Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, Bönnemann CG, Gussoni E, Denton PH, Kyriakides T, Middleton L, Hentati F, Ben Hamida M, Nonaka I, Vance JM, Kunkel LM, Ozawa E. Noguchi S, et al. Among authors: ben othmane k. Science. 1995 Nov 3;270(5237):819-22. doi: 10.1126/science.270.5237.819. Science. 1995. PMID: 7481775

9

The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).

Le Merrer M, Ben Othmane K, Stanescu V, Lyonnet S, Van Maldergem L, Royer G, Munnich A, Maroteaux P. Le Merrer M, et al. Among authors: ben othmane k. J Med Genet. 1992 Oct;29(10):713-5. doi: 10.1136/jmg.29.10.713. J Med Genet. 1992. PMID: 1433231 Free PMC article.

10

Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993.

Wood S, Ben Othmane K, Bergerheim US, Blanton SH, Bookstein R, Clarke RA, Daiger SP, Donis-Keller H, Drayna D, Kumar S, et al. Wood S, et al. Among authors: ben othmane k. Cytogenet Cell Genet. 1993;64(3-4):134-46. Cytogenet Cell Genet. 1993. PMID: 8404033 No abstract available.

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