Le Paslier D - Search Results

1

Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects.

Debrus S, Tuffery S, Matsuoka R, Galal O, Sarda P, Sauer U, Bozio A, Tanman B, Toutain A, Claustres M, Le Paslier D, Bouvagnet P. Debrus S, et al. Among authors: le paslier d. J Mol Cell Cardiol. 1997 May;29(5):1423-31. doi: 10.1006/jmcc.1997.0380. J Mol Cell Cardiol. 1997. PMID: 9201627

2

High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).

Wang I, Franco B, Ferrero GB, Chinault AC, Weissenbach J, Chumakov I, Le Paslier D, Levilliers J, Klink A, Rappold GA, Ballabio A, Petit C. Wang I, et al. Among authors: le paslier d. Genomics. 1995 Mar 20;26(2):229-38. doi: 10.1016/0888-7543(95)80205-z. Genomics. 1995. PMID: 7601447

3

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: le paslier d. Hum Mol Genet. 1994 Jun;3(6):989-93. doi: 10.1093/hmg/3.6.989. Hum Mol Genet. 1994. PMID: 7951250

4

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F, et al. Doerflinger N, et al. Among authors: le paslier d. Am J Hum Genet. 1995 May;56(5):1116-24. Am J Hum Genet. 1995. PMID: 7726167 Free PMC article.

5

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

Medhioub M, Cherif D, Benessy F, Silbermann F, Gubler MC, Le Paslier D, Cohen D, Weissenbach J, Beckmann J, Antignac C. Medhioub M, et al. Among authors: le paslier d. Genomics. 1994 Jul 15;22(2):296-301. doi: 10.1006/geno.1994.1387. Genomics. 1994. PMID: 7806215

6

Hunting 11q23 deletions with fluorescence in situ hybridization (FISH).

Cherif D, Bernard O, Paulien S, James MR, Le Paslier D, Berger R. Cherif D, et al. Among authors: le paslier d. Leukemia. 1994 Apr;8(4):578-86. Leukemia. 1994. PMID: 8152254

7

Organization of the human immunoglobulin lambda light-chain locus on chromosome 22q11.2.

Frippiat JP, Williams SC, Tomlinson IM, Cook GP, Cherif D, Le Paslier D, Collins JE, Dunham I, Winter G, Lefranc MP. Frippiat JP, et al. Among authors: le paslier d. Hum Mol Genet. 1995 Jun;4(6):983-91. doi: 10.1093/hmg/4.6.983. Hum Mol Genet. 1995. PMID: 7655473

8

A 1.7-Mb YAC contig around the human BDNF gene (11p13): integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndrome.

Rosier MF, Goguel AF, Martin A, Le Paslier D, Couillin P, Houlgatte R, Bernheim A, Auffray C, Devignes MD. Rosier MF, et al. Among authors: le paslier d. Genomics. 1994 Nov 1;24(1):69-77. doi: 10.1006/geno.1994.1583. Genomics. 1994. PMID: 7896291

9

Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome.

Imbert A, Chaffanet M, Essioux L, Noguchi T, Adélaïde J, Kerangueven F, Le Paslier D, Bonaïti-Pellié C, Sobol H, Birnbaum D, Pébusque MJ. Imbert A, et al. Among authors: le paslier d. Genomics. 1996 Feb 15;32(1):29-38. doi: 10.1006/geno.1996.0073. Genomics. 1996. PMID: 8786118

10

A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8.

Chaffanet M, Imbert A, Adélaïde J, Le Paslier D, Wagner MJ, Wells DE, Birnbaum D, Pébusque MJ. Chaffanet M, et al. Among authors: le paslier d. Cytogenet Cell Genet. 1996;72(1):63-8. doi: 10.1159/000134164. Cytogenet Cell Genet. 1996. PMID: 8565638

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