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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.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.Zeitschrift Fur Geburtshilfe Und Perinatologie|April 1, 1977
[Anhidrotic ectodermal dysplasia--Identification of heterocygote (carrier) females (author's transl)]K Messow, A Götz, J D Murken, et al.Biometrics|September 1, 1977
Assumptions for different ascertainment models in human geneticsJ S Williams, J SteneClinical 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.Human Genetics|September 22, 1977
Psoralen/UVA treatment and chromosomes. I. Aberrations and sister chromatid exchange in human lymphocytes in vitro and synergism with caffeineH Waksvik, A Brogger, J StenePageof 8