Martin J - Search Results

1

Selection of maternal human immunodeficiency virus type 1 variants in human placenta. European Network for In Utero Transmission of HIV-1.

Menu E, Mbopi-Keou FX, Lagaye S, Pissard S, Mauclère P, Scarlatti G, Martin J, Goossens M, Chaouat G, Barré-Sinoussi F. Menu E, et al. Among authors: martin j. J Infect Dis. 1999 Jan;179(1):44-51. doi: 10.1086/314542. J Infect Dis. 1999. PMID: 9841821

2

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: martin j. Mol Cell Probes. 1993 Apr;7(2):167-8. doi: 10.1006/mcpr.1993.1024. Mol Cell Probes. 1993. PMID: 8321255

3

HFE genotyping by amplification refractory mutation system-denaturing HPLC.

Pissard S, Huynh LT, Martin J, Goossens M. Pissard S, et al. Among authors: martin j. Clin Chem. 2002 May;48(5):769-72. Clin Chem. 2002. PMID: 11978606 No abstract available.

4

Human beta-globin gene polymorphisms characterized in DNA extracted from ancient bones 12,000 years old.

Béraud-Colomb E, Roubin R, Martin J, Maroc N, Gardeisen A, Trabuchet G, Goosséns M. Béraud-Colomb E, et al. Among authors: martin j. Am J Hum Genet. 1995 Dec;57(6):1267-74. Am J Hum Genet. 1995. PMID: 8533755 Free PMC article.

5

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. Among authors: martin j. Hum Genet. 1990 Sep;85(4):446-9. doi: 10.1007/BF02428305. Hum Genet. 1990. PMID: 2210768

6

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: martin j. Ann Hematol. 1992 Oct;65(4):188-92. doi: 10.1007/BF01703113. Ann Hematol. 1992. PMID: 1420507

7

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: martin j. Eur J Hum Genet. 1993;1(2):144-55. doi: 10.1159/000472401. Eur J Hum Genet. 1993. PMID: 8055323

8

Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.

Galacteros F, Girodon E, M'Rad A, Martin J, Goossens M, Jaber L, Cohen IJ, Tamary H, Goshen Y, Zaizov R, et al. Galacteros F, et al. Among authors: martin j. C R Acad Sci III. 1994 May;317(5):437-44. C R Acad Sci III. 1994. PMID: 7994622

9

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: martin j. Hum Mutat. 1992;1(3):229-39. doi: 10.1002/humu.1380010310. Hum Mutat. 1992. PMID: 1301930

10

Identification of eight mutations and three sequence variations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Ghanem N, Costes B, Girodon E, Martin J, Fanen P, Goossens M. Ghanem N, et al. Among authors: martin j. Genomics. 1994 May 15;21(2):434-6. doi: 10.1006/geno.1994.1290. Genomics. 1994. PMID: 7522211

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