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Frontiers in Molecular Neuroscience|December 25, 2013
MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-reviewAndreas J Forstner, Franziska Degenhardt, Gerhard Schratt, et al.
Biochemical and Biophysical Research Communications|December 15, 1994
Identification of genetic variation in the human serotonin 1D beta receptor geneM M Nöthen, J Erdmann, D Shimron-Abarbanell, et al.
American Journal of Medical Genetics|April 9, 1996
Lack of imprinting of the human dopamine D4 receptor (DRD4) geneS Cichon, M M Nöthen, H K Wolf, et al.
American Journal of Medical Genetics|June 1, 1993
Steinfeld syndrome: report of a second family and further delineation of a rare autosomal dominant disorderM M Nöthen, G Knöpfle, H J Födisch, et al.
Der Nervenarzt|September 6, 2002
[Genetics of bipolar affective disorders. Current status of research for identification of susceptibility genes]J Schumacher, S Cichon, M Rietschel, et al.
Annals of the New York Academy of Sciences|February 3, 1999
Genetic variation in human 5-HT receptors: potential pathogenetic and pharmacological roleM Göthert, P Propping, H Bönisch, et al.
Experimental Dermatology|February 5, 2016
Hunting the genes in male-pattern alopecia: how important are they, how close are we and what will they tell us?Stefanie Heilmann-Heimbach, Lara M Hochfeld, Ralf Paus, et al.
Biological Psychiatry|October 1, 1993
Distribution of a novel mutation in the first exon of the human dopamine D4 receptor gene in psychotic patientsM Catalano, M Nobile, E Novelli, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 3, 2018
[Drug-induced angioedema : Focus on bradykinin]B Sachs, T Meier, M M Nöthen, et al.
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