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Zeitschrift Fur Arztliche Fortbildung Und Qualitatssicherung|February 3, 2007
[Custom-made medicine: preimplantation genetic diagnosis]Karl SperlingZeitschrift Fur Arztliche Fortbildung Und Qualitatssicherung|September 11, 2002
[Preimplantation versus prenatal diagnosis--a comparison from the human genetics point of view]Karl SperlingDNA Repair|July 29, 2004
Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaksMartin Digweed, Karl SperlingGenetic Epidemiology|December 14, 2011
Evidence for an increase in trisomy 21 (Down syndrome) in Europe after the Chernobyl reactor accidentKarl Sperling, Heidemarie Neitzel, Hagen ScherbMolecular Cytogenetics|May 14, 2023
Population monitoring of trisomy 21: problems and approachesKarl Sperling, Hagen Scherb, Heidemarie NeitzelPediatric Neurology|March 23, 2004
Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephalyPavel Seeman, Katerina Gebertová, Katerina Paderová, et al.Cytogenetic and Genome Research|March 10, 2016
5-Methylcytosine-Rich Heterochromatin in the Indian MuntjacMichael Schmid, Claus Steinlein, Christian Lomb, et al.Scientific Reports|August 10, 2017
Nijmegen Breakage Syndrome fibroblasts and iPSCs: cellular models for uncovering disease-associated signaling pathways and establishing a screening platform for anti-oxidantsBarbara Mlody, Wasco Wruck, Soraia Martins, et al.Chromosoma|January 25, 2007
The granulocyte nucleus and lamin B receptor: avoiding the ovoidKatrin Hoffmann, Karl Sperling, Ada L Olins, et al.Molecular Vision|March 6, 2009
Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataractVanita Vanita, Jai Rup Singh, Daljit Singh, et al.Pageof 7