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M Poissonnier

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Archives Francaises De Pediatrie|March 1, 1978
[Mucolipidosis type I. Sialidosis due to alpha-2-6-neuraminidase deficiency with neurological symptoms]P Maroteaux, M Poissonnier, M Tondeur, et al.
Journal De Genetique Humaine|May 1, 1987
[True hermaphroditism in a child with a chimeric XX/XY chromosome, a double erythrocyte population and an unusual Lewis (a+ b+) phenotype]M Poissonnier, D Janvier, S Cabrol, et al.
Cell and Tissue Research|December 1, 1994
Expression of the alpha-subunit of glycoprotein hormones in the pars tuberalis-specific glandular cells in rat, mouse and guinea-pigM E Stoeckel, C Hindelang, M J Klein, et al.
Neuroendocrinology|December 1, 1993
Early expression of the glycoprotein hormone alpha-subunit in the pars tuberalis of the rat pituitary gland during ontogenesisM E Stoeckel, C Hindelang, M J Klein, et al.
Annales De Genetique|March 1, 1976
[Partial trisomy 21 (21q21 - 21q22.2)]M Poissonnier, B Saint-Paul, B Dutrillaux, et al.
Journal De Genetique Humaine|December 1, 1983
[Familial cancer of the colon without polyposis and the familial cancer syndrome. Apropos of 2 cases over 3 generations]M Poissonnier, J Andrieu, J D Gardon, et al.
Biochemical and Biophysical Research Communications|April 16, 1985
Cystathionine beta synthase: gene dosage effect in trisomy 21B Chadefaux, M O Rethoré, O Raoul, et al.
Cancer Genetics and Cytogenetics|March 1, 1993
Acute lymphoblastic leukemia with trisomy 21 constitutional mosaicismC Léonard, M R Avalos, F Miélot, et al.
Human Genetics|January 1, 1984
Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221B Chadefaux, D Allard, M O Rethoré, et al.
American Journal of Human Genetics|March 1, 1990
Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21J L Blouin, Z Rahmani, Z Chettouh, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Archives Francaises De Pediatrie|March 1, 1978
[Mucolipidosis type I. Sialidosis due to alpha-2-6-neuraminidase deficiency with neurological symptoms]P Maroteaux, M Poissonnier, M Tondeur, et al.
Journal De Genetique Humaine|May 1, 1987
[True hermaphroditism in a child with a chimeric XX/XY chromosome, a double erythrocyte population and an unusual Lewis (a+ b+) phenotype]M Poissonnier, D Janvier, S Cabrol, et al.
Cell and Tissue Research|December 1, 1994
Expression of the alpha-subunit of glycoprotein hormones in the pars tuberalis-specific glandular cells in rat, mouse and guinea-pigM E Stoeckel, C Hindelang, M J Klein, et al.
Neuroendocrinology|December 1, 1993
Early expression of the glycoprotein hormone alpha-subunit in the pars tuberalis of the rat pituitary gland during ontogenesisM E Stoeckel, C Hindelang, M J Klein, et al.
Annales De Genetique|March 1, 1976
[Partial trisomy 21 (21q21 - 21q22.2)]M Poissonnier, B Saint-Paul, B Dutrillaux, et al.
Journal De Genetique Humaine|December 1, 1983
[Familial cancer of the colon without polyposis and the familial cancer syndrome. Apropos of 2 cases over 3 generations]M Poissonnier, J Andrieu, J D Gardon, et al.
Biochemical and Biophysical Research Communications|April 16, 1985
Cystathionine beta synthase: gene dosage effect in trisomy 21B Chadefaux, M O Rethoré, O Raoul, et al.
Cancer Genetics and Cytogenetics|March 1, 1993
Acute lymphoblastic leukemia with trisomy 21 constitutional mosaicismC Léonard, M R Avalos, F Miélot, et al.
Human Genetics|January 1, 1984
Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221B Chadefaux, D Allard, M O Rethoré, et al.
American Journal of Human Genetics|March 1, 1990
Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21J L Blouin, Z Rahmani, Z Chettouh, et al.
Pageof 2