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S Stengel-Rutkowski

Showing results (51-60 of 63) with videos related to

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Annales De Genetique|January 1, 1992
Different risks in two familial translocations t(9;12) with similar breakpointsA T Midro, S Stengel-Rutkowski, M Krajewska-Walasek, et al.
Deutsche Medizinische Wochenschrift (1946)|January 17, 1975
[Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)]K Harzer, S Stengel-Rutkowski, E O Gley, et al.
Geburtshilfe Und Frauenheilkunde|July 1, 1980
[Prenatal diagnosis in parents with a balanced structural chromosome aberration (author's transl)]A Wirtz, S Stengel-Rutkowski, J Stene, et al.
Annales De Genetique|August 6, 1999
Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literatureT Eggermann, R Schubert, H Engels, et al.
Human Genetics|May 1, 1996
Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typingT Eggermann, H Engels, B Moskalonek, et al.
European Journal of Pediatrics|July 1, 1981
New chromosomal dysmorphic syndromes. 4. Trisomy 12pS Stengel-Rutkowski, A Albert, J D Murken, et al.
Cytogenetics and Cell Genetics|January 1, 1979
A (3;17) balanced translocation, 46 chromosomes. Repository identification No. GM-2808S Stengel-Rutkowski, A Wirtz, J P Murken, et al.
MMW, Munchener Medizinische Wochenschrift|April 18, 1980
[Prenatal diagnosis--a corner-post in preventive medicine]J D Murken, A Albert, M Endres, et al.
Clinical Genetics|August 1, 1996
Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the motherC Apacik, M Cohen, M Jakobeit, et al.
American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Annales De Genetique|January 1, 1992
Different risks in two familial translocations t(9;12) with similar breakpointsA T Midro, S Stengel-Rutkowski, M Krajewska-Walasek, et al.
Deutsche Medizinische Wochenschrift (1946)|January 17, 1975
[Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)]K Harzer, S Stengel-Rutkowski, E O Gley, et al.
Geburtshilfe Und Frauenheilkunde|July 1, 1980
[Prenatal diagnosis in parents with a balanced structural chromosome aberration (author's transl)]A Wirtz, S Stengel-Rutkowski, J Stene, et al.
Annales De Genetique|August 6, 1999
Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literatureT Eggermann, R Schubert, H Engels, et al.
Human Genetics|May 1, 1996
Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typingT Eggermann, H Engels, B Moskalonek, et al.
European Journal of Pediatrics|July 1, 1981
New chromosomal dysmorphic syndromes. 4. Trisomy 12pS Stengel-Rutkowski, A Albert, J D Murken, et al.
Cytogenetics and Cell Genetics|January 1, 1979
A (3;17) balanced translocation, 46 chromosomes. Repository identification No. GM-2808S Stengel-Rutkowski, A Wirtz, J P Murken, et al.
MMW, Munchener Medizinische Wochenschrift|April 18, 1980
[Prenatal diagnosis--a corner-post in preventive medicine]J D Murken, A Albert, M Endres, et al.
Clinical Genetics|August 1, 1996
Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the motherC Apacik, M Cohen, M Jakobeit, et al.
American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.
Pageof 7