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Xenobiotica; the Fate of Foreign Compounds in Biological Systems|August 1, 1988
The transfer and metabolism of 7-ethoxycoumarin and androstenedione during the in vitro perfusion of the human placental lobuleA J Cummings, D K Copas, A C Kaelin, et al.The Journal of Investigative Dermatology|November 17, 2001
The relation between melanocortin 1 receptor genotype and experimentally assessed ultraviolet radiation sensitivityN Flanagan, A J Ray, C Todd, et al.Clinical Endocrinology|April 13, 2000
Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?A Koziell, E Charmandari, P C Hindmarsh, et al.Acta Dermato-Venereologica|May 23, 2013
The importance of a full clinical examination: assessment of index lesions referred to a skin cancer clinic without a total body skin examination would miss one in three melanomasR Benjamin Aldridge, Lisa Naysmith, Ee Ting Ooi, et al.BMC Genetics|January 1, 2010
Genetic determinants of hair and eye colours in the Scottish and Danish populationsJonas Mengel-From, Terence H Wong, Niels Morling, et al.BMC Medicine|October 26, 2023
Shoulder replacement surgery's rising demand, inequality of provision, and variation in outcomes: cohort study using Hospital Episode Statistics for EnglandEpaminondas Markos Valsamis, Rafael Pinedo-Villanueva, Adrian Sayers, et al.Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association|January 1, 1978
Sex hormone changes underlying menstrual disturbances on haemodialysisV J Wass, J A Wass, L Rees, et al.The Journal of Investigative Dermatology|September 21, 2000
The spectrum of mitochondrial DNA deletions is a ubiquitous marker of ultraviolet radiation exposure in human skinA J Ray, R Turner, O Nikaido, et al.Pediatric Nephrology (Berlin, Germany)|February 1, 1993
Prospective cytomegalovirus surveillance in paediatric renal transplant patientsS Iragorri, D Pillay, M Scrine, et al.The Journal of Investigative Dermatology|October 16, 2004
Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hairAneta Ringholm, Janis Klovins, Richard Rudzish, et al.Pageof 84