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Neurology|April 14, 2004
CCM1 mutation screen of sporadic cases with cerebral cavernous malformationsD J Verlaan, S B Laurent, U Sure, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 27, 1998
[Sorsby's fundus dystrophy. A genetically homogeneous disease]U Felbor, B H Weber
Cytogenetic and Genome Research|October 4, 2003
The rare human fragile site 16BU Felbor, W Feichtinger, M Schmid
Genome Research|December 1, 1995
Genomic organization of the human tissue inhibitor of metalloproteinases-3 (TIMP3)H Stöhr, K Roomp, U Felbor, et al.
Cell Structure and Function|July 8, 2000
Collagen XVIII/endostatin structure and functional role in angiogenesisU K Zatterstrom, U Felbor, N Fukai, et al.
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