Cohen D - Search Results

1

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: cohen d. Genomics. 1994 Jul 15;22(2):296-301. doi: 10.1006/geno.1994.1387. Genomics. 1994. PMID: 7806215

2

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: cohen d. Genomics. 1994 Jul 15;22(2):388-96. doi: 10.1006/geno.1994.1400. Genomics. 1994. PMID: 7806226

3

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: cohen d. Am J Hum Genet. 1994 Apr;54(4):687-94. Am J Hum Genet. 1994. PMID: 8128967 Free PMC article.

4

Targeted development of microsatellite markers from inter-Alu amplification of YAC clones.

de Souza AP, Allamand V, Richard I, Brenguier L, Chumakov I, Cohen D, Beckmann JS. de Souza AP, et al. Among authors: cohen d. Genomics. 1994 Jan 15;19(2):391-3. doi: 10.1006/geno.1994.1079. Genomics. 1994. PMID: 8188274

5

The gene for creatine kinase, mitochondrial 2 (sarcomeric; CKMT2), maps to chromosome 5q13.3.

Richard I, Devaud C, Cherif D, Cohen D, Beckmann JS. Richard I, et al. Among authors: cohen d. Genomics. 1993 Oct;18(1):134-6. doi: 10.1006/geno.1993.1437. Genomics. 1993. PMID: 8276398

6

Mapping of two chromosome 15 microsatellites.

Fougerousse F, Richard I, Broux O, Cohen D, Beckmann JS. Fougerousse F, et al. Among authors: cohen d. Genomics. 1992 Jul;13(3):903-4. doi: 10.1016/0888-7543(92)90184-t. Genomics. 1992. PMID: 1639425 No abstract available.

7

Cloning the human major histocompatibility complex in YACs.

Abderrahim H, Sambucy JL, Iris F, Ougen P, Billault A, Chumakov IM, Dausset J, Cohen D, Le Paslier D. Abderrahim H, et al. Among authors: cohen d. Genomics. 1994 Oct;23(3):520-7. doi: 10.1006/geno.1994.1538. Genomics. 1994. PMID: 7851878

8

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: cohen d. Hum Mol Genet. 1994 Jan;3(1):99-106. doi: 10.1093/hmg/3.1.99. Hum Mol Genet. 1994. PMID: 8162060

9

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: cohen d. Genomics. 1995 Sep 1;29(1):163-9. doi: 10.1006/geno.1995.1227. Genomics. 1995. PMID: 8530067

10

A simple method for prenatal diagnosis of trisomy 21 on uncultured amniocytes.

Romana SP, Tachdjian G, Druart L, Cohen D, Berger R, Chérif D. Romana SP, et al. Among authors: cohen d. Eur J Hum Genet. 1993;1(3):245-51. doi: 10.1159/000472418. Eur J Hum Genet. 1993. PMID: 8044650

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