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S Gilgenkrantz

Showing results (61-70 of 129) with videos related to

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American Journal of Medical Genetics|September 1, 1982
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathyS Gilgenkrantz, C Vigneron, M J Gregoire, et al.
Annales De Genetique|January 1, 1992
Incontinentia pigmenti (type 1) and X;5 translocationP Bitoun, C Philippe, M Cherif, et al.
Annales De Genetique|January 1, 1985
Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?S Gilgenkrantz, P Tridon, N Pinel-Briquel, et al.
Annales De Genetique|March 1, 1971
[The Dr syndrome. Study of a further case (46, XX, 14r)]S Gilgenkrantz, C Cabrol, C Lausecker, et al.
Journal De Genetique Humaine|September 1, 1981
[Translocation (3;20) and anorchism]S Gilgenkrantz, F Cruz-Marin, M J Gregoire, et al.
Journal De Genetique Humaine|June 1, 1985
[Prenatal diagnosis of triploidy. I. Echographic, clinical and anatomic studies]S Gilgenkrantz, P Droulle, M Schweitzer, et al.
Journal De Genetique Humaine|December 1, 1980
[Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study]F Cruz-Marin, S Gilgenkrantz, M J Gregoire, et al.
Revue Francaise De Transfusion Et Immuno-Hematologie|February 1, 1981
A study of immuno-genetic tracers in a pair of discordant twins with blood chimeraS Gilgenkrantz, C Janot, P Perrier, et al.
Annales De Genetique|September 1, 1970
[Syndrome 47, XXYY, 13-, 14-, t(13q14q)+]S Gilgenkrantz, J P Grilliat, D A Vautrin, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1972
[Isolation of a cell clone secreting human somatotropic hormone in tissue culture]P Hartemann, P Paysant, F Belleville, et al.
Pageof 13

Showing results (61-70 of 129) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|September 1, 1982
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathyS Gilgenkrantz, C Vigneron, M J Gregoire, et al.
Annales De Genetique|January 1, 1992
Incontinentia pigmenti (type 1) and X;5 translocationP Bitoun, C Philippe, M Cherif, et al.
Annales De Genetique|January 1, 1985
Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11?S Gilgenkrantz, P Tridon, N Pinel-Briquel, et al.
Annales De Genetique|March 1, 1971
[The Dr syndrome. Study of a further case (46, XX, 14r)]S Gilgenkrantz, C Cabrol, C Lausecker, et al.
Journal De Genetique Humaine|September 1, 1981
[Translocation (3;20) and anorchism]S Gilgenkrantz, F Cruz-Marin, M J Gregoire, et al.
Journal De Genetique Humaine|June 1, 1985
[Prenatal diagnosis of triploidy. I. Echographic, clinical and anatomic studies]S Gilgenkrantz, P Droulle, M Schweitzer, et al.
Journal De Genetique Humaine|December 1, 1980
[Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study]F Cruz-Marin, S Gilgenkrantz, M J Gregoire, et al.
Revue Francaise De Transfusion Et Immuno-Hematologie|February 1, 1981
A study of immuno-genetic tracers in a pair of discordant twins with blood chimeraS Gilgenkrantz, C Janot, P Perrier, et al.
Annales De Genetique|September 1, 1970
[Syndrome 47, XXYY, 13-, 14-, t(13q14q)+]S Gilgenkrantz, J P Grilliat, D A Vautrin, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1972
[Isolation of a cell clone secreting human somatotropic hormone in tissue culture]P Hartemann, P Paysant, F Belleville, et al.
Pageof 13