Abdelhak S - Search Results

1

Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy gene.

Melki J, Burlet P, Clermont O, Pascal F, Paul B, Abdelhak S, Sherrington R, Gurling H, Nakamura Y, Weissenbach J, et al. Melki J, et al. Among authors: abdelhak s. Genomics. 1993 Mar;15(3):521-4. doi: 10.1006/geno.1993.1103. Genomics. 1993. PMID: 8096827

2

In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3.

Mattei MG, Melki J, Bachelot MF, Abdelhak S, Burlet P, Frézal J, Munnich A. Mattei MG, et al. Among authors: abdelhak s. Cytogenet Cell Genet. 1991;57(2-3):112-3. doi: 10.1159/000133125. Cytogenet Cell Genet. 1991. PMID: 1914518

3

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q.

Melki J, Abdelhak S, Sheth P, Bachelot MF, Burlet P, Marcadet A, Aicardi J, Barois A, Carriere JP, Fardeau M, et al. Melki J, et al. Among authors: abdelhak s. Nature. 1990 Apr 19;344(6268):767-8. doi: 10.1038/344767a0. Nature. 1990. PMID: 1970420

4

Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14. The French Spinal Muscular Atrophy Investigators.

Melki J, Sheth P, Abdelhak S, Burlet P, Bachelot MF, Lathrop MG, Frezal J, Munnich A. Melki J, et al. Among authors: abdelhak s. Lancet. 1990 Aug 4;336(8710):271-3. doi: 10.1016/0140-6736(90)91803-i. Lancet. 1990. PMID: 1973971

5

Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5.

Sheth P, Abdelhak S, Bachelot MF, Burlet P, Masset M, Hillaire D, Clerget-Darpoux F, Frézal J, Lathrop GM, Munnich A, et al. Sheth P, et al. Among authors: abdelhak s. Am J Hum Genet. 1991 Apr;48(4):764-8. Am J Hum Genet. 1991. PMID: 2014799 Free PMC article.

6

Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

Melki J, Abdelhak S, Burlet P, Raclin V, Kaplan J, Spiegel R, Gilgenkrantz S, Philip N, Chauvet ML, Dumez Y, et al. Melki J, et al. Among authors: abdelhak s. J Med Genet. 1992 Mar;29(3):171-4. doi: 10.1136/jmg.29.3.171. J Med Genet. 1992. PMID: 1348092 Free PMC article.

7

A PstI polymorphism at the D5S39 locus.

Abdelhak S, Melki J, Bachelot MF, Burlet P, Sheth P, Frézal J, Munnich A. Abdelhak S, et al. Nucleic Acids Res. 1990 Sep 25;18(18):5580. doi: 10.1093/nar/18.18.5580-a. Nucleic Acids Res. 1990. PMID: 1977124 Free PMC article.

8

Trinucleotide repeat polymorphism at the D5S556 locus.

Burlet P, Abdelhak S, Pascal F, Clermont O, Paul B, Munnich A, Melki J. Burlet P, et al. Among authors: abdelhak s. Hum Mol Genet. 1993 Aug;2(8):1328. doi: 10.1093/hmg/2.8.1328. Hum Mol Genet. 1993. PMID: 8401523 No abstract available.

9

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.

Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Levi-Acobas F, Cruaud C, Le Merrer M, Mathieu M, König R, Vigneron J, Weissenbach J, Petit C, Weil D. Abdelhak S, et al. Hum Mol Genet. 1997 Dec;6(13):2247-55. doi: 10.1093/hmg/6.13.2247. Hum Mol Genet. 1997. PMID: 9361030

10

Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome.

Kalatzis V, Abdelhak S, Compain S, Vincent C, Petit C. Kalatzis V, et al. Among authors: abdelhak s. Genomics. 1996 Jun 15;34(3):422-5. doi: 10.1006/geno.1996.0307. Genomics. 1996. PMID: 8786145

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