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S Gilgenkrantz

Showing results (11-20 of 129) with videos related to

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Annales De Genetique|December 9, 2003
The history of cytogenetics. Portraits of some pioneersS Gilgenkrantz, E M Rivera
Annales De Genetique|January 1, 1983
[Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells]I Tejada, J Boué, S Gilgenkrantz
Clinical Genetics|February 1, 1990
On the familial occurrence of congenital bilateral absence of vas deferensS Gilgenkrantz, P Guillemin, B Kimmel
American Journal of Medical Genetics|April 15, 1994
X inactivation in Rett syndrome: a preliminary study showing partial preferential inactivation of paternal X with the M27 beta probeP Camus, N Abbadi, S Gilgenkrantz
Archives Francaises De Pediatrie|November 1, 1975
[Cat eye syndrome with pituitary dwarfism and normal mental development]M Pierson, S Gilgenkrantz, M Saborio
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1972
[Waardenburg's syndrome and extra chromosome fragment. Study of a family]J Cordier, A Raspiller, S Gilgenkrantz
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Chromosome rearrangements and human gene mappingS Gilgenkrantz, C Philippe, M Chery
Annales De Genetique|September 1, 1973
[13q+ chromosome due to a probable translocation of a supernumerary Y]S Gilgenkrantz, M Pierson, G Mauuary
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1976
[Action of 5-bromodeoxyuridine as a function of time on the aspect of chromosomes. Attempt at interpretation]S Gilgenkrantz, M J Gregoire, F Streiff
Bulletin De L'Association Des Anatomistes|June 1, 1976
[Cytogenetic studies in spontaneous abortions]S Gilgenkrantz, M J Gregoire, F Streiff
Pageof 13

Showing results (11-20 of 129) with videos related to

Sort By:
Pageof 13
Annales De Genetique|December 9, 2003
The history of cytogenetics. Portraits of some pioneersS Gilgenkrantz, E M Rivera
Annales De Genetique|January 1, 1983
[Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells]I Tejada, J Boué, S Gilgenkrantz
Clinical Genetics|February 1, 1990
On the familial occurrence of congenital bilateral absence of vas deferensS Gilgenkrantz, P Guillemin, B Kimmel
American Journal of Medical Genetics|April 15, 1994
X inactivation in Rett syndrome: a preliminary study showing partial preferential inactivation of paternal X with the M27 beta probeP Camus, N Abbadi, S Gilgenkrantz
Archives Francaises De Pediatrie|November 1, 1975
[Cat eye syndrome with pituitary dwarfism and normal mental development]M Pierson, S Gilgenkrantz, M Saborio
Bulletins Et Memoires De La Societe Francaise D'Ophtalmologie|January 1, 1972
[Waardenburg's syndrome and extra chromosome fragment. Study of a family]J Cordier, A Raspiller, S Gilgenkrantz
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Chromosome rearrangements and human gene mappingS Gilgenkrantz, C Philippe, M Chery
Annales De Genetique|September 1, 1973
[13q+ chromosome due to a probable translocation of a supernumerary Y]S Gilgenkrantz, M Pierson, G Mauuary
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1976
[Action of 5-bromodeoxyuridine as a function of time on the aspect of chromosomes. Attempt at interpretation]S Gilgenkrantz, M J Gregoire, F Streiff
Bulletin De L'Association Des Anatomistes|June 1, 1976
[Cytogenetic studies in spontaneous abortions]S Gilgenkrantz, M J Gregoire, F Streiff
Pageof 13