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Calcified Tissue International|June 11, 2009
Mutational analysis of the PHEX gene: novel point mutations and detection of large deletions by MLPA in patients with X-linked hypophosphatemic ricketsS Clausmeyer, V Hesse, P C Clemens, et al.Life Sciences|January 1, 1989
Acute effects of marijuana smoke on complex operant behavior in rhesus monkeysG E Schulze, D E McMillan, J R Bailey, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 1, 1996
Iodine-123-iodo-lisuride SPECT in Parkinson's diseaseM Cordes, J Hierholzer, L Schelosky, et al.Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|February 1, 1987
(Z)-17 beta-hydroxy-17 alpha-(2-[125I]iodovinyl)-4-estren-3-one: a new specific gamma-emitting ligand for determination of progesterone receptorH J Grill, A Heubner, K Pollow, et al.Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 17, 2009
New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumourK Frank-Raue, J Döhring, G Scheumann, et al.Nuklearmedizin. Nuclear Medicine|August 1, 1995
[Brain SPECT with 123I-lisuride in patients with Parkinson's disease and controls]J Hierholzer, M Cordes, L Schelosky, et al.Journal of Molecular Medicine (Berlin, Germany)|November 3, 2001
A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotypeE Schulze-Bahr, M Schwarz, S Hauenschild, et al.Journal of the American Academy of Dermatology|November 2, 2007
Basal cell carcinoma in childhood: case report and literature reviewJohn R Griffin, Philip R Cohen, Jaime A Tschen, et al.Clinical Genetics|August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?C Evers, P H Heidemann, D Dunstheimer, et al.Clinical Genetics|February 6, 2004
Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutationH Wedekind, M Schwarz, S Hauenschild, et al.Pageof 33