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Human Genetics|June 1, 1994
Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomesR Viersbach, G Schwanitz, M M NöthenFEBS Letters|March 7, 1994
Human complement component C8. Molecular basis of the beta-chain polymorphismG Dewald, S Hemmer, M M NöthenBiochemical and Biophysical Research Communications|July 15, 1993
Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 BG Dewald, M M Nöthen, S CichonHuman Heredity|November 1, 1994
A common Ser/Thr polymorphism in the perforin-homologous region of human complement component C7G Dewald, M M Nöthen, K RütherFrontiers in Behavioral Neuroscience|May 21, 2010
New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?Vanessa Nieratschker, Markus M Nöthen, Marcella RietschelTrends in Molecular Medicine|September 3, 2011
Breakthroughs in the genetics of orofacial cleftingElisabeth Mangold, Kerstin U Ludwig, Markus M NöthenDer Nervenarzt|February 14, 2019
[Breakthrough in understanding the molecular causes of psychiatric disorders]Markus M Nöthen, Franziska Degenhardt, Andreas J ForstnerImmunology|September 11, 2012
Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnosticsBritta Haenisch, Markus M Nöthen, Gerhard J MolderingsMedizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|July 8, 2026
Polygenic risk scores in clinical applications - opportunities and challengesJohannes Schumacher, Markus M Nöthen, Stefanie Heilmann-HeimbachAnnales De Genetique|January 1, 1993
Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counsellingT Eggermann, M M Nöthen, P Propping, et al.Pageof 88