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Ginecologia Y Obstetricia De Mexico|September 1, 1993
[Ligation of the hypogastric arteries. Analysis of 4000 cases]E Torreblanca Neve, G Merchan Escalante, M A Walter Tordecillas, et al.American Journal of Human Genetics|February 17, 2001
Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1R A Saleem, S Banerjee-Basu, F B Berry, et al.Human Genetics|December 1, 1994
The immunoglobulin heavy chain and disease association: application to pemphigus vulgarisW T Gibson, M A Walter, A R Ahmed, et al.Cell|July 11, 1998
The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalusT Kume, K Y Deng, V Winfrey, et al.Archives of Environmental Contamination and Toxicology|July 1, 1981
Acute impact of an organophosphorus insecticide on microbes and small invertebrates of a mangrove estuaryS Y Newell, K E Cooksey, J W Fell, et al.Genomics|April 1, 1991
Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombinationJ C Benger, I Teshima, M A Walter, et al.European Journal of Clinical Investigation|May 19, 2004
Radioiodine therapy in hyperthyroidism: inverse correlation of pretherapeutic iodine uptake level and post-therapeutic outcomeM A Walter, M Christ-Crain, B Eckard, et al.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|May 20, 2005
[Is the Canadian CT head rule for minor head injury applicable for patients in Germany?]P M Schlegel, M A Walter, S P Kloska, et al.Human Molecular Genetics|August 7, 2001
Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndromeM Priston, K Kozlowski, D Gill, et al.European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.Pageof 23