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S Stengel-Rutkowski

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Human Mutation|January 1, 1996
A familial deletion in the Prader-Willi syndrome region including the imprinting control regionS Schuffenhauer, T Buchholz, S Stengel-Rutkowski, et al.
Fortschritte Der Medizin|January 15, 1981
[Transsexualism and the H-Y antigen]W Eicher, M Spoljar, J D Murken, et al.
MMW, Munchener Medizinische Wochenschrift|May 7, 1976
[The chromosome bands. Significance for clinical and cytogenetic research (author's transl)]S Stengel-Rutkowski, J U Walther, A Wirtz, et al.
Clinical Genetics|October 1, 1992
Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the riskS Stengel-Rutkowski, K Lohse, C Herzog, et al.
Human Genetics|January 28, 1976
Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11)S Stengel-Rutkowski, H Zankl, A Rodewald, et al.
Geburtshilfe Und Frauenheilkunde|June 1, 1980
[Transexuality and X-Y antigen (author's transl)]W Eicher, M Spoljar, K Richter, et al.
European Journal of Pediatrics|February 8, 1979
New chromosomal dysmorphic syndromes. 3. Partial trisomy 3qS Stengel-Rutkowski, J D Murken, V Pilar, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Tetrasomy 18p caused by paternal meiotic nondisjunctionT Eggermann, H Engels, C Apacik, et al.
European Journal of Pediatrics|October 12, 1977
New chromosomal dysmorphic syndromes. 2. Trisomy 10pS Stengel-Rutkowski, J D Murken, R Frankenberger, et al.
Lancet (London, England)|July 20, 1974
Letter: Klinefelter's syndrome in a fetusJ D Murken, S Stengel-Rutkowski, J U Walther, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Human Mutation|January 1, 1996
A familial deletion in the Prader-Willi syndrome region including the imprinting control regionS Schuffenhauer, T Buchholz, S Stengel-Rutkowski, et al.
Fortschritte Der Medizin|January 15, 1981
[Transsexualism and the H-Y antigen]W Eicher, M Spoljar, J D Murken, et al.
MMW, Munchener Medizinische Wochenschrift|May 7, 1976
[The chromosome bands. Significance for clinical and cytogenetic research (author's transl)]S Stengel-Rutkowski, J U Walther, A Wirtz, et al.
Clinical Genetics|October 1, 1992
Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the riskS Stengel-Rutkowski, K Lohse, C Herzog, et al.
Human Genetics|January 28, 1976
Aspermia, associated with a presumably balanced X/autosomal translocation karyotype 46, Y, t (X;5) (q28;q11)S Stengel-Rutkowski, H Zankl, A Rodewald, et al.
Geburtshilfe Und Frauenheilkunde|June 1, 1980
[Transexuality and X-Y antigen (author's transl)]W Eicher, M Spoljar, K Richter, et al.
European Journal of Pediatrics|February 8, 1979
New chromosomal dysmorphic syndromes. 3. Partial trisomy 3qS Stengel-Rutkowski, J D Murken, V Pilar, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Tetrasomy 18p caused by paternal meiotic nondisjunctionT Eggermann, H Engels, C Apacik, et al.
European Journal of Pediatrics|October 12, 1977
New chromosomal dysmorphic syndromes. 2. Trisomy 10pS Stengel-Rutkowski, J D Murken, R Frankenberger, et al.
Lancet (London, England)|July 20, 1974
Letter: Klinefelter's syndrome in a fetusJ D Murken, S Stengel-Rutkowski, J U Walther, et al.
Pageof 7