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Page 1
Problems in detecting mosaic DNA methylation in Angelman syndrome.
Horsthemke B, Lich C, Buiting K, Achmann R, Aulehla-Scholz C, Baumer A, Bürger J, Dworniczak B, Gläser D, Holinski-Feder E, Janssen B, Kleinle S, Kochhan L, Krasemann E, Kraus C, Kroisel P, Plendl H, Purmann S, Sander G, Skladny H, Spitzer E, Thamm-Mücke B, Varon-Mateeva R, Weinhäusel A, Weirich H. Horsthemke B, et al. Among authors: purmann s. Eur J Hum Genet. 2003 Dec;11(12):913-5. doi: 10.1038/sj.ejhg.5201078. Eur J Hum Genet. 2003. PMID: 14523374 No abstract available.
New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome.
Beygo J, Küchler A, Gillessen-Kaesbach G, Albrecht B, Eckle J, Eggermann T, Gellhaus A, Kanber D, Kordaß U, Lüdecke HJ, Purmann S, Rossier E, van de Nes J, van der Werf IM, Wenzel M, Wieczorek D, Horsthemke B, Buiting K. Beygo J, et al. Among authors: purmann s. Eur J Hum Genet. 2017 Aug;25(8):935-945. doi: 10.1038/ejhg.2017.91. Epub 2017 Jun 21. Eur J Hum Genet. 2017. PMID: 28635951 Free PMC article.
hSKCa3: a candidate gene for schizophrenia?
Meissner B, Purmann S, Schürmann M, Zühlke C, Lencer R, Arolt V, Müller-Myhsok B, Morris-Rosendahl DJ, Schwinger E. Meissner B, et al. Among authors: purmann s. Psychiatr Genet. 1999 Jun;9(2):91-6. Psychiatr Genet. 1999. PMID: 10412188
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease.
Arolt V, Lencer R, Nolte A, Müller-Myhsok B, Purmann S, Schürmann M, Leutelt J, Pinnow M, Schwinger E. Arolt V, et al. Among authors: purmann s. Am J Med Genet. 1996 Nov 22;67(6):564-79. doi: 10.1002/(SICI)1096-8628(19961122)67:6<564::AID-AJMG10>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8950416
15 results