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Genetic Testing and Molecular Biomarkers|July 17, 2009
GPR143 mutational analysis in two Italian families with X-linked ocular albinismLucia Micale, Bartolomeo Augello, Carmela Fusco, et al.
BMC Medical Genetics|August 7, 2013
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic settingValentina Gatta, Elena Gennaro, Sara Franchi, et al.
The Journal of Molecular Diagnostics : JMD|April 12, 2008
A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotypeMassimiliano Cecconi, Francesca Forzano, Rosanna Rinaldi, et al.
IEEE Journal of Biomedical and Health Informatics|July 15, 2015
Adaptive Mathematical Model of Tumor Response to Radiotherapy Based on CBCT DataA Belfatto, M Riboldi, D Ciardo, et al.
Human Reproduction (Oxford, England)|December 13, 2006
Ultrastructure of human mature oocytes after slow cooling cryopreservation using different sucrose concentrationsS A Nottola, G Macchiarelli, G Coticchio, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|November 30, 2006
Sentinel lymph node biopsy for high risk cutaneous squamous cell carcinoma: case series and review of the literatureC Renzi, A Caggiati, T J Mannooranparampil, et al.
Zebrafish|April 23, 2020
Zebrafish ambra1a and ambra1b Silencing Affect Heart DevelopmentGiacomo Meneghetti, Tatjana Skobo, Martina Chrisam, et al.
European Journal of Anaesthesiology|April 26, 2019
Tidal volume challenge to predict fluid responsiveness in the operating room: An observational studyAntonio Messina, Claudia Montagnini, Gianmaria Cammarota, et al.
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