Showing results (301-310 of 723) with videos related to
Sort By:
Pageof 73
American Journal of Medical Genetics. Part A|January 25, 2005
Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA)Cecilia Giunta, Ann Randolph, Lihadh I Al-Gazali, et al.American Journal of Medical Genetics. Part A|March 29, 2005
Malpuech syndrome: three patients and a reviewW S Kerstjens-Frederikse, H G Brunner, C M L van Dael, et al.Experimental Cell Research|February 1, 1991
Urokinase-type and tissue-type plasminogen activators are essential for in vitro invasion of human melanoma cellsA Meissauer, M D Kramer, M Hofmann, et al.International Journal of Oncology|May 10, 2011
Adhesive function of newcastle-disease virus hemagglutinin in tumor-host interactionK Jurianz, C Haas, M Hubbe, et al.Wiener Klinische Wochenschrift|January 1, 1996
Intensive care management of acute pancreatitis: recognition of patients at high risk of developing severe or fatal complicationsP Kaufmann, G Hofmann, K H Smolle, et al.Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14B H W Faas, J Van Der Deure, M I Wunderink, et al.Acta Biomaterialia|January 7, 2014
The formation of an anti-restenotic/anti-thrombotic surface by immobilization of nitric oxide synthase on a metallic carrierM Alagem-Shafir, E Kivovich, I Tzchori, et al.Science (New York, N.Y.)|June 20, 1997
Large porous particles for pulmonary drug deliveryD A Edwards, J Hanes, G Caponetti, et al.Brain Research. Developmental Brain Research|July 6, 2005
Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresisBert van der Zwaag, J Peter H Burbach, Han G Brunner, et al.Muscle & Nerve|March 1, 1992
Eye movement disorder: an early expression of the myotonic dystrophy gene?J P ter Bruggen, C C Tijssen, H G Brunner, et al.Pageof 73