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S Gilgenkrantz

Showing results (41-50 of 129) with videos related to

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Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1970
[Study of electrophoretic mobility of human lymphocytes before and after in vitro culture]S Gilgenkrantz, J F Stoltz, F Streiff, et al.
Journal De Genetique Humaine|July 1, 1984
[Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families]S Gilgenkrantz, J Boué, M J Grégoire, et al.
Journal De Genetique Humaine|December 1, 1985
[Prenatal diagnosis of triploidy. II. Biological studies]S Gilgenkrantz, P Mujica, P Perrier, et al.
Journal De Genetique Humaine|September 1, 1989
[Balanced X-autosomal translocation and mental retardation. Mapping mental retardation linked to X (excluding fragile X)]M Teboul, P Mujica, M Chery, et al.
Journal of Medical Genetics|September 1, 1989
3M dwarfism: a study of two further sibsM Feldmann, S Gilgenkrantz, S Parisot, et al.
La Nouvelle Presse Medicale|March 3, 1973
[Chromosome mosaics 47, XYY-45, XO. 2 cases with different sex]S Gilgenkrantz, C Cabrol, D Simon, et al.
Human Genetics|February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.
Journal De Genetique Humaine|January 1, 1988
[Robertsonian translocation and genetic counseling]L F Formiga, B Le Marec, F Serville, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1970
[Variations of antigen "A" during acute myeloblastic leukemia]F Streiff, C Salmon, A Peters, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1970
[Technic of fetal sex determination in amniotic fluid]S Gilgenkrantz, C Vigneron, P Landes, et al.
Pageof 13

Showing results (41-50 of 129) with videos related to

Sort By:
Pageof 13
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1970
[Study of electrophoretic mobility of human lymphocytes before and after in vitro culture]S Gilgenkrantz, J F Stoltz, F Streiff, et al.
Journal De Genetique Humaine|July 1, 1984
[Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families]S Gilgenkrantz, J Boué, M J Grégoire, et al.
Journal De Genetique Humaine|December 1, 1985
[Prenatal diagnosis of triploidy. II. Biological studies]S Gilgenkrantz, P Mujica, P Perrier, et al.
Journal De Genetique Humaine|September 1, 1989
[Balanced X-autosomal translocation and mental retardation. Mapping mental retardation linked to X (excluding fragile X)]M Teboul, P Mujica, M Chery, et al.
Journal of Medical Genetics|September 1, 1989
3M dwarfism: a study of two further sibsM Feldmann, S Gilgenkrantz, S Parisot, et al.
La Nouvelle Presse Medicale|March 3, 1973
[Chromosome mosaics 47, XYY-45, XO. 2 cases with different sex]S Gilgenkrantz, C Cabrol, D Simon, et al.
Human Genetics|February 1, 1986
A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probesS Gilgenkrantz, M E Briquel, J L Mandel, et al.
Journal De Genetique Humaine|January 1, 1988
[Robertsonian translocation and genetic counseling]L F Formiga, B Le Marec, F Serville, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1970
[Variations of antigen "A" during acute myeloblastic leukemia]F Streiff, C Salmon, A Peters, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1970
[Technic of fetal sex determination in amniotic fluid]S Gilgenkrantz, C Vigneron, P Landes, et al.
Pageof 13