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Investigation of complement C4B deficiency in schizophrenia.
Schroers R, Nöthen MM, Rietschel M, Albus M, Maier W, Schwab S, Wildenauer D, Fimmers R, Propping P, Dewald G. Schroers R, et al. Among authors: fimmers r. Hum Hered. 1997 Sep-Oct;47(5):279-82. doi: 10.1159/000154424. Hum Hered. 1997. PMID: 9358016
Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.
Cichon S, Nöthen MM, Stöber G, Schroers R, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Wildenauer D, Fimmers R, Propping P. Cichon S, et al. Among authors: fimmers r. Am J Med Genet. 1996 Jul 26;67(4):424-8. doi: 10.1002/(SICI)1096-8628(19960726)67:4<424::AID-AJMG21>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8837716
Apolipoprotein E genotype distribution in schizophrenia.
Zhu S, Nöthen MM, Uhlhaas S, Rietschel M, Körner J, Lanczik M, Fimmers R, Propping P. Zhu S, et al. Among authors: fimmers r. Psychiatr Genet. 1996 Summer;6(2):75-9. doi: 10.1097/00041444-199622000-00007. Psychiatr Genet. 1996. PMID: 8840393
Association versus linkage studies in psychosis genetics.
Nöthen MM, Propping P, Fimmers R. Nöthen MM, et al. Among authors: fimmers r. J Med Genet. 1993 Aug;30(8):634-7. doi: 10.1136/jmg.30.8.634. J Med Genet. 1993. PMID: 8411047 Free PMC article. No abstract available.
435 results