Goossens M - Search Results

1

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

2

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: m rad a, goossens m. C R Acad Sci III. 1994 May;317(5):437-44. C R Acad Sci III. 1994. PMID: 7994622

3

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

4

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

5

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

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: goossens 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

Progress in the DNA diagnosis of hemophilias.

Goossens M, Ghanem N. Goossens M, et al. Ann Hematol. 1991 Apr;62(4):115-8. doi: 10.1007/BF01702924. Ann Hematol. 1991. PMID: 1674433 Review.

8

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: goossens m. Hum Genet. 1990 Sep;85(4):446-9. doi: 10.1007/BF02428305. Hum Genet. 1990. PMID: 2210768

9

Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains.

Riou J, Pissard S, Goossens M, Wajcman H. Riou J, et al. Among authors: goossens m. Int J Lab Hematol. 2015 Apr;37(2):279-86. doi: 10.1111/ijlh.12286. Epub 2014 Aug 11. Int J Lab Hematol. 2015. PMID: 25130136

10

A one-step real-time PCR assay for rapid prenatal diagnosis of sickle cell disease and detection of maternal contamination.

Costa C, Pissard S, Girodon E, Huot D, Goossens M. Costa C, et al. Among authors: goossens m. Mol Diagn. 2003;7(1):45-8. doi: 10.1007/BF03260020. Mol Diagn. 2003. PMID: 14529320

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