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S Gilgenkrantz

Showing results (21-30 of 129) with videos related to

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Journal De Genetique Humaine|March 1, 1976
[Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study]S Gilgenkrantz, R Walbaum, G Mauuary, et al.
Bulletin De La Societe Francaise De Dermatologie Et De Syphiligraphie|January 1, 1970
[Immunosuppressive agents and cytogenetics]S Gilgenkrantz, M Weber, M Grandidier, et al.
Revue Medicale De Liege|June 1, 1976
[A case of trisomy 8 in mosaic 47, XY, +8/46, XY]M Pierson, S Gilgenkrantz, O Brocard, et al.
Progress in Clinical and Biological Research|January 1, 1981
Cytogenetic and antigenic studies in a pair of twins: a normal boy and a trisomic 21 girl with chimeraS Gilgenkrantz, C Marchal, P Wendremaire, et al.
Humangenetik|January 1, 1975
[Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)]S Gilgenkrantz, G Mauuary, B Dutrillaux, et al.
Bulletin Des Societes D'Ophtalmologie De France|August 1, 1982
[Aniridia and deletion of chromosome 11 (loss of the band p13)--apropos of a case]A Raspiller, S Gilgenkrantz, C Pernot, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1974
[Inactivation of one X chromosome in the woman]S Gilgenkrantz, P Alexandre, M Saborio, et al.
Archives Francaises De Pediatrie|February 1, 1985
[Partial trisomy of chromosome 3 resulting from paternal translocation]M Cointin, D Olive, S Gilgenkrantz, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|May 10, 1973
[Erythrocytic enzymes and chromosome aberrations. Contribution to the establishment of the human factorial chart]C Vigneron, S Gilgenkrantz, C Cabrol, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The Noonan syndrome. The Nancy experience revisitedM Chery, C Philippe, A M Worms, et al.
Pageof 13

Showing results (21-30 of 129) with videos related to

Sort By:
Pageof 13
Journal De Genetique Humaine|March 1, 1976
[Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study]S Gilgenkrantz, R Walbaum, G Mauuary, et al.
Bulletin De La Societe Francaise De Dermatologie Et De Syphiligraphie|January 1, 1970
[Immunosuppressive agents and cytogenetics]S Gilgenkrantz, M Weber, M Grandidier, et al.
Revue Medicale De Liege|June 1, 1976
[A case of trisomy 8 in mosaic 47, XY, +8/46, XY]M Pierson, S Gilgenkrantz, O Brocard, et al.
Progress in Clinical and Biological Research|January 1, 1981
Cytogenetic and antigenic studies in a pair of twins: a normal boy and a trisomic 21 girl with chimeraS Gilgenkrantz, C Marchal, P Wendremaire, et al.
Humangenetik|January 1, 1975
[Late replication and X-autosome traslocation a case with banding patterns autoradiographic and B.U.D.R. studies (author's transl)]S Gilgenkrantz, G Mauuary, B Dutrillaux, et al.
Bulletin Des Societes D'Ophtalmologie De France|August 1, 1982
[Aniridia and deletion of chromosome 11 (loss of the band p13)--apropos of a case]A Raspiller, S Gilgenkrantz, C Pernot, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1974
[Inactivation of one X chromosome in the woman]S Gilgenkrantz, P Alexandre, M Saborio, et al.
Archives Francaises De Pediatrie|February 1, 1985
[Partial trisomy of chromosome 3 resulting from paternal translocation]M Cointin, D Olive, S Gilgenkrantz, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|May 10, 1973
[Erythrocytic enzymes and chromosome aberrations. Contribution to the establishment of the human factorial chart]C Vigneron, S Gilgenkrantz, C Cabrol, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The Noonan syndrome. The Nancy experience revisitedM Chery, C Philippe, A M Worms, et al.
Pageof 13