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Journal of Genetic Counseling|November 18, 2015
Experience with genetic counseling: the adolescent perspectiveAmanda Pichini, Cheryl Shuman, Karen Sappleton, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 27, 2009
An autophagic vacuolar myopathy-like disorder presenting as nonimmune hydrops in a female fetusCharis Kepron, Andrea Blumenthal, David Chitayat, et al.Journal of Genetic Counseling|March 3, 2026
Examining aspects of job satisfaction associated with burnout and factors related to turnover intention in genetic counselorsKaitlin J Stanley, Ian M MacFarlane, Susan Randall Armel, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 14, 2003
Single nucleotide polymorphism of the human kallikrein-2 gene highly correlates with serum human kallikrein-2 levels and in combination enhances prostate cancer detectionRobert K Nam, William W Zhang, John Trachtenberg, et al.International Journal of Radiation Oncology, Biology, Physics|February 18, 2004
Polarographic electrode study of tumor oxygenation in clinically localized prostate cancerChris Parker, Michael Milosevic, Ants Toi, et al.Clinical Case Reports|April 27, 2023
Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case reportYiming Wang, Joanna Lazier, Diane Myles-Reid, et al.The Journal of Urology|March 7, 2006
A novel serum marker, total prostate secretory protein of 94 amino acids, improves prostate cancer detection and helps identify high grade cancers at diagnosisRobert K Nam, Jonathan R Reeves, Ants Toi, et al.Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada|April 27, 2017
Modern-day prostate cancer is not meaningfully associated with lower urinary tract symptoms: Analysis of a propensity score-matched cohortAmar Bhindi, Bimal Bhindi, Girish S Kulkarni, et al.Human Molecular Genetics|January 30, 2013
Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndromeKaren Buysse, Moniek Riemersma, Gareth Powell, et al.The Journal of Urology|July 27, 2016
Limitations in Predicting Organ Confined Prostate Cancer in Patients with Gleason Pattern 4 on Biopsy: Implications for Active SurveillanceNathan Perlis, Rashid Sayyid, Andrew Evans, et al.Pageof 53