Research output per year
Research output per year
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Dive into the research topics where Monika Hagedorn-Greiwe is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation
Teber, Ö. A., Gillessen-Kaesbach, G., Fischer, S., Böhringer, S., Albrecht, B., Albert, A., Arslan-Kirchner, M., Haan, E., Hagedorn-Greiwe, M., Hammans, C., Henn, W., Hinkel, G. K., König, R., Kunstmann, E., Kunze, J., Neumann, L. M., Prott, E. C., Rauch, A., Rott, H. D., Seidel, H., & 5 others, 11.2004, In: European Journal of Human Genetics. 12, 11, p. 879-890 12 p.Research output: Journal Articles › Journal articles › Research › peer-review
107 Citations (Scopus) -
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, D. P., Bätge, B. & Brinckmann, J., 01.10.2003, In: British Journal of Dermatology. 149, 4, p. 850-852 3 p.Research output: Journal Articles › Journal articles › Research › peer-review
12 Citations (Scopus) -
Erratum: Das kind mit behinderung in familie und gesellschaft (Monatsschrift fur Kinderheilkunde)
Thyen, U., Hagedorn-Greiwe, M. & Queisser-Luft, A., 2002, In: Monatsschrift fur Kinderheilkunde. 150, 10, p. 1179 1 p.Research output: Journal Articles › Comments/Debates
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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, X. O., Kömpf, D. & Ozelius, L., 15.11.1998, In: Genomics. 54, 1, p. 176-177 2 p.Research output: Journal Articles › Journal articles › Research › peer-review
28 Citations (Scopus)