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Clinical Genetics|November 8, 2012
Skirting the pitfalls: a clear-cut nomenclature for H3K4 methyltransferasesN Bögershausen, E Bruford, B WollnikDer Internist|June 27, 2018
[Modern genetic counselling : Practical aspects exemplified by hypertrophic cardiomyopathy]F Czepluch, G Hasenfuß, B WollnikBiophysical Journal|July 24, 1998
Activation and inactivation of homomeric KvLQT1 potassium channelsM Pusch, R Magrassi, B Wollnik, et al.Human Molecular Genetics|May 1, 1997
Identification of functionally important regions of the muscular chloride channel CIC-1 by analysis of recessive and dominant myotonic mutationsB Wollnik, C Kubisch, K Steinmeyer, et al.Biochemical and Biophysical Research Communications|July 30, 1993
Hyperosmotic stress induces immediate-early gene expression in ventricular adult cardiomyocytesB Wollnik, C Kubisch, A Maass, et al.Tissue Antigens|January 15, 2009
Extended genetic analysis of BTNL2 in sarcoidosisY Li, S Pabst, S Lokhande, et al.Prenatal Diagnosis|April 4, 2003
A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish familyB Karaman, B Wollnik, H Ermiş, et al.European Journal of Neurology|January 11, 2002
CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptorU Utku, Y Celik, O Uyguner, et al.Pageof 4