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Immunogenetics|April 8, 2017
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencingJanine Altmüller, Britta Haenisch, Amit Kawalia, et al.Schizophrenia Bulletin|March 4, 2025
Schizotypy, Psychosis Proneness, and the Polygenic Risk for Schizophrenia and ResilienceTina Meller, Clara Lundberg, Carlo Maj, et al.Clinical Dysmorphology|April 1, 1995
Desbuquois syndrome: three further cases and review of the literatureG Gillessen-Kaesbach, P Meinecke, M G Ausems, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|May 1, 1994
[Pemphigus chronicus benignus familiaris (Hailey-Hailey disease) and bipolar affective disease in 3 members of a family]M Wilk, M Rietschel, J Körner, et al.Psychiatric Genetics|January 1, 1996
Apolipoprotein E genotype distribution in schizophreniaS Zhu, M M Nöthen, S Uhlhaas, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 27, 2004
Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) geneDorothea Gadzicki, Kirsten R Müller-Vahl, Daniela Heller, et al.Clinical and Experimental Dermatology|March 27, 2015
A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicismS Redler, S M Pasternack, S Wolf, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|July 20, 2010
Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadiasMarkus Draaken, Judith Proske, Charlotte Schramm, et al.Molecular Psychiatry|July 8, 1999
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteersE G Jönsson, M M Nöthen, F Grünhage, et al.The British Journal of Psychiatry : the Journal of Mental Science|July 1, 1993
Familial cosegregation of affective disorder and Hailey-Hailey diseaseJ Körner, M Rietschel, M M Nöthen, et al.Pageof 88