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S Gilgenkrantz

Showing results (51-60 of 129) with videos related to

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La Nouvelle Presse Medicale|January 17, 1976
[XXYY chromosomal constitution recognised during the 1st year of life]S Gilgenkrantz, G Mauuary, M Saborio, et al.
Annales De Genetique|January 1, 1989
A case of Alagille's syndrome with translocation (4;14) (q21;q21)P Mujica, A Morali, M Vidailhet, et al.
Journal D'Urologie Et De Nephrologie|April 1, 1972
[Chronic kidney failure in a mentally deficient patient with a chromosome abnormality (Triplo X)]C Huriet, C Fontenaille, S Gilgenkrantz, et al.
Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.
Nature|October 13, 1983
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour associationC Huerre, S Despoisse, S Gilgenkrantz, et al.
Human Genetics|February 1, 1996
X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probeP Camus, N Abbadi, M C Perrier, et al.
Pediatrie|January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]C Pernot, A M Worms, F Marçon, et al.
Annales De Genetique|December 1, 1972
[Deletion of the short arm of chromosome 18 due to t(22-;18p+) translocation with IgA deficiency. Cytogenetic study with autoradiography and fluorescence]S Gilgenkrantz, J M Charles, C Cabrol, et al.
Journal De Genetique Humaine|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, et al.
Journal De Genetique Humaine|July 1, 1984
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]S Gilgenkrantz, M J Gregoire, M Chery, et al.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
La Nouvelle Presse Medicale|January 17, 1976
[XXYY chromosomal constitution recognised during the 1st year of life]S Gilgenkrantz, G Mauuary, M Saborio, et al.
Annales De Genetique|January 1, 1989
A case of Alagille's syndrome with translocation (4;14) (q21;q21)P Mujica, A Morali, M Vidailhet, et al.
Journal D'Urologie Et De Nephrologie|April 1, 1972
[Chronic kidney failure in a mentally deficient patient with a chromosome abnormality (Triplo X)]C Huriet, C Fontenaille, S Gilgenkrantz, et al.
Journal De Genetique Humaine|March 1, 1983
[Chromosome 11 and cancer]M J Gregoire, C Pernot, F Himont, et al.
Nature|October 13, 1983
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour associationC Huerre, S Despoisse, S Gilgenkrantz, et al.
Human Genetics|February 1, 1996
X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probeP Camus, N Abbadi, M C Perrier, et al.
Pediatrie|January 1, 1989
[Noonan's syndrome and its cardiovascular dysplasia. Apropos of 64 cases]C Pernot, A M Worms, F Marçon, et al.
Annales De Genetique|December 1, 1972
[Deletion of the short arm of chromosome 18 due to t(22-;18p+) translocation with IgA deficiency. Cytogenetic study with autoradiography and fluorescence]S Gilgenkrantz, J M Charles, C Cabrol, et al.
Journal De Genetique Humaine|January 1, 1989
[Clinical and biological studies of 14 cases of the Prader-Labhart-Willi syndrome]P Mujica, B Leheup, S Gilgenkrantz, et al.
Journal De Genetique Humaine|July 1, 1984
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]S Gilgenkrantz, M J Gregoire, M Chery, et al.
Pageof 13