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The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Four families with loss of function mutations of the thyrotropin receptorN de Roux, M Misrahi, R Brauner, et al.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae|August 7, 2003
[Propagation of hepatitis E virus in several cell lines including human embryo lung diploid cell KMB17]G Y Le, J Wu, Y B Ma, et al.
Arthritis and Rheumatism|July 29, 2006
In vivo and in vitro characterization of skeletal muscle metabolism in patients with statin-induced adverse effectsS Guis, D Figarella-Branger, J P Mattei, et al.
Transplantation|April 30, 1999
The xenotransplantation of goat and human hematopoietic cells to sheep fetusesG Colas, P Hollands, A Locatelli, et al.
Journal of Medical Genetics|September 26, 2013
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndromeF Brioude, I Oliver-Petit, A Blaise, et al.
Anatomia Clinica|January 1, 1985
Study of the mandible under static constraints by holographic interferometry. New biomechanical deductionsJ C Ferré, R Legoux, J L Helary, et al.
The Journal of Antimicrobial Chemotherapy|February 11, 2021
Impact of extracorporeal membrane oxygenation (ECMO) support on piperacillin exposure in septic patients: a case-control studyP Fillâtre, F Lemaitre, N Nesseler, et al.
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