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Annales De Genetique
|
December 9, 2003
The history of cytogenetics. Portraits of some pioneers
S 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 deferens
S 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 probe
P 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 mapping
S 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
Page
of 13
Search research articles
Search
Showing results (11-20 of 129) with videos related to
Sort By:
Page
of 13
Annales De Genetique
|
December 9, 2003
The history of cytogenetics. Portraits of some pioneers
S 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 deferens
S 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 probe
P 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 mapping
S 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
Page
of 13