Hazan J - Search Results

1

Wunderle V, Dib C, Fizames C, Morisette J, Hazan J, Hansmann I, Whitehouse D, Vergnaud G, Weissenbach J. Wunderle V, et al. Among authors: hazan j. Eur J Hum Genet. 1994;2(3):242-3. Eur J Hum Genet. 1994. PMID: 7834300 No abstract available.

2

A comprehensive genetic map of the human genome based on 5,264 microsatellites.

Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J. Dib C, et al. Among authors: hazan j. Nature. 1996 Mar 14;380(6570):152-4. doi: 10.1038/380152a0. Nature. 1996. PMID: 8600387

3

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers.

Hazan J, Dubay C, Pankowiak MP, Becuwe N, Weissenbach J. Hazan J, et al. Genomics. 1992 Feb;12(2):183-9. doi: 10.1016/0888-7543(92)90364-x. Genomics. 1992. PMID: 1740328

4

A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.

Vincent P, Plauchu H, Hazan J, Fauré S, Weissenbach J, Godet J. Vincent P, et al. Among authors: hazan j. Hum Mol Genet. 1995 May;4(5):945-9. doi: 10.1093/hmg/4.5.945. Hum Mol Genet. 1995. PMID: 7633456

5

Mapping of microsatellite markers in the Alagille region and screening of microdeletions by genotyping 23 patients.

Deleuze JF, Hazan J, Dhorne S, Weissenbach J, Hadchouel M. Deleuze JF, et al. Among authors: hazan j. Eur J Hum Genet. 1994;2(3):185-90. doi: 10.1159/000472362. Eur J Hum Genet. 1994. PMID: 7834278

6

Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy.

Vicart P, Dupret JM, Hazan J, Li Z, Gyapay G, Krishnamoorthy R, Weissenbach J, Fardeau M, Paulin D. Vicart P, et al. Among authors: hazan j. Hum Genet. 1996 Oct;98(4):422-9. doi: 10.1007/s004390050233. Hum Genet. 1996. PMID: 8792816

7

Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

Paternotte C, Rudnicki D, Fizames C, Davoine CS, Mavel D, Dürr A, Samson D, Marquette C, Muselet D, Vega-Czarny N, Drouot N, Voit T, Fontaine B, Gyapay G, Auburger G, Weissenbach J, Hazan J. Paternotte C, et al. Among authors: hazan j. Genome Res. 1998 Nov;8(11):1216-27. doi: 10.1101/gr.8.11.1216. Genome Res. 1998. PMID: 9847083 Free PMC article.

8

A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

Hazan J, Davoine CS, Mavel D, Fonknechten N, Paternotte C, Fizames C, Cruaud C, Samson D, Muselet D, Vega-Czarny N, Brice A, Gyapay G, Heilig R, Fontaine B, Weissenbach J. Hazan J, et al. Genomics. 1999 Sep 15;60(3):309-19. doi: 10.1006/geno.1999.5932. Genomics. 1999. PMID: 10493830

9

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.

Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J. Hazan J, et al. Nat Genet. 1993 Oct;5(2):163-7. doi: 10.1038/ng1093-163. Nat Genet. 1993. PMID: 8252041

10

Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.

De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C. De Jonghe P, et al. Among authors: hazan j. Eur J Hum Genet. 1996;4(5):260-6. doi: 10.1159/000472212. Eur J Hum Genet. 1996. PMID: 8946171

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