Vidaud M - Search Results

1

Three point mutations in the CFTR gene in French cystic fibrosis patients: identification by denaturing gradient gel electrophoresis.

Vidaud M, Fanen P, Martin J, Ghanem N, Nicolas S, Goossens M. Vidaud M, et al. Hum Genet. 1990 Sep;85(4):446-9. doi: 10.1007/BF02428305. Hum Genet. 1990. PMID: 2210768

2

A comprehensive scanning method for rapid detection of beta-globin gene mutations and polymorphisms.

Ghanem N, Girodon E, Vidaud M, Martin J, Fanen P, Plassa F, Goossens M. Ghanem N, et al. Among authors: vidaud m. Hum Mutat. 1992;1(3):229-39. doi: 10.1002/humu.1380010310. Hum Mutat. 1992. PMID: 1301930

3

Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.

Gandrille S, Vidaud M, Aiach M, Alhenc-Gelas M, Fischer AM, Gouault-Heilman M, Toulon P, Fiessinger JN, Goossens M. Gandrille S, et al. Among authors: vidaud m. Hum Mutat. 1992;1(6):491-500. doi: 10.1002/humu.1380010607. Hum Mutat. 1992. PMID: 1301959

4

Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions.

Fanen P, Ghanem N, Vidaud M, Besmond C, Martin J, Costes B, Plassa F, Goossens M. Fanen P, et al. Among authors: vidaud m. Genomics. 1992 Jul;13(3):770-6. doi: 10.1016/0888-7543(92)90152-i. Genomics. 1992. PMID: 1379210

5

Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variants.

Girodon E, Ghanem N, Vidaud M, Riou J, Martin J, Galactéros F, Goossens M. Girodon E, et al. Among authors: vidaud m. Ann Hematol. 1992 Oct;65(4):188-92. doi: 10.1007/BF01703113. Ann Hematol. 1992. PMID: 1420507

6

Exhaustive screening of exon 10 CFTR gene mutations and polymorphisms by denaturing gradient gel electrophoresis: applications to genetic counselling in cystic fibrosis.

Ghanem N, Fanen P, Martin J, Conteville P, Yahia-Cherif Z, Vidaud M, Goossens M. Ghanem N, et al. Among authors: vidaud m. Mol Cell Probes. 1992 Feb;6(1):27-31. doi: 10.1016/0890-8508(92)90068-9. Mol Cell Probes. 1992. PMID: 1545831

7

Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French population.

Vidaud M, Ferec C, Attree O, Pascal O, Guillermit H, Ghanem N, Martin J, Moisan JP, Feingold J, Goossens M. Vidaud M, et al. Hum Genet. 1990 Sep;85(4):434-5. doi: 10.1007/BF02428302. Hum Genet. 1990. PMID: 1976598

8

Twenty-four novel hemophilia B mutations revealed by rapid scanning of the whole factor IX gene in a French population sample.

Ghanem N, Costes B, Martin J, Vidaud M, Rothschild C, Foyer-Gazengel C, Goossens M. Ghanem N, et al. Among authors: vidaud m. Eur J Hum Genet. 1993;1(2):144-55. doi: 10.1159/000472401. Eur J Hum Genet. 1993. PMID: 8055323

9

Direct carrier detection and prenatal diagnosis of Sicilian and Spanish (delta beta)zero-thalassemias.

Ghanem N, Vidaud M, Plassa F, Martin J, Goossens M. Ghanem N, et al. Among authors: vidaud m. Mol Cell Probes. 1993 Apr;7(2):167-8. doi: 10.1006/mcpr.1993.1024. Mol Cell Probes. 1993. PMID: 8321255

10

A new strategy for direct detection of beta-thalassemia mutations. Experience of the Créteil Center.

Goossens M, Fanen P, Attree O, Vidaud M. Goossens M, et al. Among authors: vidaud m. Ann N Y Acad Sci. 1990;612:74-80. doi: 10.1111/j.1749-6632.1990.tb24292.x. Ann N Y Acad Sci. 1990. PMID: 2291576 No abstract available.

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