Hagedorn-Greiwe M - Search Results

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Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation.

Tao J, Van Esch H, Hagedorn-Greiwe M, Hoffmann K, Moser B, Raynaud M, Sperner J, Fryns JP, Schwinger E, Gécz J, Ropers HH, Kalscheuer VM. Tao J, et al. Among authors: hagedorn greiwe m. Am J Hum Genet. 2004 Dec;75(6):1149-54. doi: 10.1086/426460. Am J Hum Genet. 2004. PMID: 15499549 Free PMC article.

Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.

Teber OA, Gillessen-Kaesbach G, Fischer S, Böhringer S, Albrecht B, Albert A, Arslan-Kirchner M, Haan E, Hagedorn-Greiwe M, Hammans C, Henn W, Hinkel GK, König R, Kunstmann E, Kunze J, Neumann LM, Prott EC, Rauch A, Rott HD, Seidel H, Spranger S, Sprengel M, Zoll B, Lohmann DR, Wieczorek D. Teber OA, et al. Among authors: hagedorn greiwe m. Eur J Hum Genet. 2004 Nov;12(11):879-90. doi: 10.1038/sj.ejhg.5201260. Eur J Hum Genet. 2004. PMID: 15340364

Reduced skin thickness: a new minor diagnostic criterion for the classical and hypermobility types of Ehlers-Danlos syndrome.

Eisenbeiss C, Martinez A, Hagedorn-Greiwe M, Reinhardt DP, Bätge B, Brinckmann J. Eisenbeiss C, et al. Among authors: hagedorn greiwe m. Br J Dermatol. 2003 Oct;149(4):850-2. doi: 10.1046/j.1365-2133.2003.05439.x. Br J Dermatol. 2003. PMID: 14616379

Familial coexistence of primary antiphospholipid syndrome and factor VLeiden.

Schütt M, Klüter H, Hagedorn-Greiwe M, Fehm HL, Wiedemann GJ. Schütt M, et al. Among authors: hagedorn greiwe m. Lupus. 1998;7(3):176-82. doi: 10.1191/096120398678919967. Lupus. 1998. PMID: 9607641

Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus.

Klein C, Vieregge P, Heide W, Kemper B, Hagedorn-Greiwe M, Hagenah J, Vollmer C, Breakefield XO, Kömpf D, Ozelius L. Klein C, et al. Among authors: hagedorn greiwe m. Genomics. 1998 Nov 15;54(1):176-7. doi: 10.1006/geno.1998.5535. Genomics. 1998. PMID: 9806847 No abstract available.

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