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Reumatologia Clinica|August 19, 2017
Renal transplantation in systemic lupus erythematosus: Comparison of graft survival with other causes of end-stage renal diseaseGabriel Horta-Baas, Adolfo Camargo-Coronel, Dafhne Guadalupe Miranda-Hernández, et al.Journal of Inherited Metabolic Disease|April 23, 2003
Plasma pipecolic acid is frequently elevated in non-peroxisomal diseaseJ C M Baas, R van de Laar, L Dorland, et al.Molecular Syndromology|October 4, 2021
Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic CardiomyopathyMonica Martin-de Saro, Zyndia Compean, Karina Aguilar, et al.BMC Bioinformatics|December 16, 2010
Initial steps towards a production platform for DNA sequence analysis on the gridAngela C M Luyf, Barbera D C van Schaik, Michel de Vries, et al.Psychopharmacology|May 6, 2009
Validating a human model for anxiety using startle potentiated by cue and context: the effects of alprazolam, pregabalin, and diphenhydramineJ M P Baas, N Mol, J L Kenemans, et al.Origins of Life and Evolution of the Biosphere : the Journal of the International Society for the Study of the Origin of Life|January 1, 1985
Photochemical reactions in interstellar grains photolysis of CO, NH3, and H2OV K Agarwal, W Schutte, J M Greenberg, et al.Nature Genetics|September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contracturesG J Jöbsis, H Keizers, J P Vreijling, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 14, 2003
Dihydropyrimidinase deficiency and severe 5-fluorouracil toxicityAndré B P van Kuilenburg, Rutger Meinsma, Bernard A Zonnenberg, et al.Adipocyte|April 21, 2017
A novel and robust method for testing bimodality and characterizing porcine adipocytes of adipose tissue of 5 purebred lines of pigEric D Testroet, Peter Sherman, Chad Yoder, et al.European Journal of Human Genetics : EJHG|August 23, 2012
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndromeGordana Raca, Becky S Baas, Salman Kirmani, et al.Pageof 215