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Acta Neuropathologica|September 18, 1997
Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparationsT Liehr, H Grehl, B RautenstraussJournal of the Peripheral Nervous System : JPNS|August 26, 2000
Expression pattern of the peripheral myelin protein 22kDa (PMP22) in neural and non-neural tissue types of adult wildtype and Trembler mice--a comparative studyB Rautenstrauss, U Zechner, H Hameister, et al.Neurogenetics|May 18, 1999
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosisC Fuchs, T Liehr, S Ozbey, et al.Journal of Neuroscience Research|December 15, 1995
Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine developmentD Baechner, T Liehr, H Hameister, et al.Neuromuscular Disorders : NMD|January 1, 1997
Clinical and morphological phenotype of HMSN 1A mosaicismH Grehl, B Rautenstrauss, T Liehr, et al.Human Genetics|July 1, 1996
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversionT Liehr, B Rautenstrauss, H Grehl, et al.Journal of Neuroscience Research|November 24, 1999
Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell linesK Hühne, O Park, T Liehr, et al.International Journal of Oncology|May 3, 2011
The peripheral myelin protein 22 kDa (PMP22) gene is amplified in cell lines derived from glioma and osteogenic sarcomaT Liehr, O Park, B Feuerstein, et al.Genome Research|October 6, 1999
Localization of mariner DNA transposons in the human genome by PRINSL T Reiter, T Liehr, B Rautenstrauss, et al.Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.Pageof 20