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Mitochondrion|June 10, 2014
Heterologous expression from the human D-Loop in organelloC B Jackson, C Zbinden, S Gallati, et al.Mitochondrion|February 5, 2011
Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegiaA Schaller, R Desetty, D Hahn, et al.Klinische Padiatrie|September 17, 2005
[Menkes' disease: heterozygosity testing by quantitative real-time PCR and the dilemma of therapeutic support]O Rittinger, G Sander, A Schaller, et al.European Journal of Pediatrics|November 14, 2015
A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephalyC B Jackson, M F Bauer, A Schaller, et al.American Journal of Medical Genetics. Part A|July 9, 2011
Contiguous ∼16 Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethalityA Nicoulaz, F Rubi, L Lieder, et al.Gynakologisch-Geburtshilfliche Rundschau|January 1, 1994
[The Wertheim picture. Biography of a painting]A SchallerWiener Klinische Wochenschrift|August 11, 1978
[The Second Gynaecological Department of Vienna University (author's transl)]A SchallerWiener Klinische Wochenschrift|May 12, 1989
[Uterine growth in the endometrium active phase]A SchallerPhytochemistry|February 14, 1998
Action of proteolysis-resistant systemin analogues in wound signallingA SchallerPageof 26