Le Paslier D - Search Results

1

A 11 Mb YAC-based contig spanning the familial juvenile nephronophthisis region (NPH1) located on chromosome 2q.

Konrad M, Saunier S, Silbermann F, Benessy F, Le Paslier D, Weissenbach J, Broyer M, Gubler MC, Antignac C. Konrad M, et al. Among authors: le paslier d. Genomics. 1995 Dec 10;30(3):514-20. doi: 10.1006/geno.1995.1272. Genomics. 1995. PMID: 8825638

2

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

3

A YAC contig in 6p23 based on sequence tagged sites.

Nemani M, Cherif D, Chesne H, Pelandakis M, Ougen P, Berger R, Weissenbach J, Le Paslier D, Cohen D, Cann HM. Nemani M, et al. Among authors: le paslier d. Genomics. 1994 Jul 15;22(2):388-96. doi: 10.1006/geno.1994.1400. Genomics. 1994. PMID: 7806226

4

Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis.

Konrad M, Saunier S, Heidet L, Silbermann F, Benessy F, Calado J, Le Paslier D, Broyer M, Gubler MC, Antignac C. Konrad M, et al. Among authors: le paslier d. Hum Mol Genet. 1996 Mar;5(3):367-71. doi: 10.1093/hmg/5.3.367. Hum Mol Genet. 1996. PMID: 8852662

5

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

6

Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.

Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K. Bashir R, et al. Among authors: le paslier d. Genomics. 1996 Apr 1;33(1):46-52. doi: 10.1006/geno.1996.0157. Genomics. 1996. PMID: 8617508

7

Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42-43.

Barrat FJ, Auloge L, Pastural E, Lagelouse RD, Vilmer E, Cant AJ, Weissenbach J, Le Paslier D, Fischer A, de Saint Basile G. Barrat FJ, et al. Among authors: le paslier d. Am J Hum Genet. 1996 Sep;59(3):625-32. Am J Hum Genet. 1996. PMID: 8751864 Free PMC article.

8

Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers.

Clermont O, Burlet P, Burglen L, Lefebvre S, Pascal F, McPherson J, Wasmuth JJ, Cohen D, Le Paslier D, Weissenbach J, et al. Clermont O, et al. Among authors: le paslier d. Am J Hum Genet. 1994 Apr;54(4):687-94. Am J Hum Genet. 1994. PMID: 8128967 Free PMC article.

9

Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35.

Lu-Kuo JM, Le Paslier D, Weissenbach J, Chumakov I, Cohen D, Ward DC. Lu-Kuo JM, et al. Among authors: le paslier d. Hum Mol Genet. 1994 Jan;3(1):99-106. doi: 10.1093/hmg/3.1.99. Hum Mol Genet. 1994. PMID: 8162060

10

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

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