Chaïb H - Search Results

1

A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).

Guilford P, Dodé C, Crozet F, Blanchard S, Chaïb H, Levilliers J, Levi-Acobas F, Weil D, Weissenbach J, Cohen D, et al. Guilford P, et al. Among authors: chaib h. Genomics. 1995 Sep 1;29(1):163-9. doi: 10.1006/geno.1995.1227. Genomics. 1995. PMID: 8530067

2

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval.

Chaïb H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgon A, Petit C. Chaïb H, et al. Hum Mol Genet. 1994 Dec;3(12):2219-22. doi: 10.1093/hmg/3.12.2219. Hum Mol Genet. 1994. PMID: 7881423

3

Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2).

Dodé C, Weil D, Levilliers J, Crozet F, Chaïb H, Levi-Acobas F, Guilford P, Petit C. Dodé C, et al. Among authors: chaib h. Genomics. 1998 Jan 1;47(1):125-30. doi: 10.1006/geno.1997.5081. Genomics. 1998. PMID: 9465305

4

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.

Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C. Guilford P, et al. Among authors: chaib h. Hum Mol Genet. 1994 Jun;3(6):989-93. doi: 10.1093/hmg/3.6.989. Hum Mol Genet. 1994. PMID: 7951250

5

A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.

Chaïb H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselet J, Petit C. Chaïb H, et al. Hum Mol Genet. 1996 Jan;5(1):155-8. doi: 10.1093/hmg/5.1.155. Hum Mol Genet. 1996. PMID: 8789454

6

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

Chaib H, Place C, Salem N, Dodé C, Chardenoux S, Weissenbach J, el Zir E, Loiselet J, Petit C. Chaib H, et al. Hum Mol Genet. 1996 Jul;5(7):1061-4. doi: 10.1093/hmg/5.7.1061. Hum Mol Genet. 1996. PMID: 8817348

7

A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21.

Chaïb H, Kaplan J, Gerber S, Vincent C, Ayadi H, Slim R, Munnich A, Weissenbach J, Petit C. Chaïb H, et al. Hum Mol Genet. 1997 Jan;6(1):27-31. doi: 10.1093/hmg/6.1.27. Hum Mol Genet. 1997. PMID: 9002666

8

Connexin 26 gene linked to a dominant deafness.

Denoyelle F, Lina-Granade G, Plauchu H, Bruzzone R, Chaïb H, Lévi-Acobas F, Weil D, Petit C. Denoyelle F, et al. Among authors: chaib h. Nature. 1998 May 28;393(6683):319-20. doi: 10.1038/30639. Nature. 1998. PMID: 9620796 No abstract available.

9

Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.

Adato A, Kalinski H, Weil D, Chaib H, Korostishevsky M, Bonne-Tamir B. Adato A, et al. Among authors: chaib h. Am J Hum Genet. 1999 Jul;65(1):261-5. doi: 10.1086/302438. Am J Hum Genet. 1999. PMID: 10364543 Free PMC article. No abstract available.

10

Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.

Boulila-Elgaïed A, Masmoudi S, Drira M, Gouia M, Chaib H, Petit C, Ayadi H. Boulila-Elgaïed A, et al. Among authors: chaib h. Arch Inst Pasteur Tunis. 1997 Jan-Apr;74(1-2):5-8. Arch Inst Pasteur Tunis. 1997. PMID: 15945170

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