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Human Genetics|December 12, 2018
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairmentJeroen J Smits, Jaap Oostrik, Andy J Beynon, et al.
Brain : a Journal of Neurology|February 2, 2023
SMPD4 regulates mitotic nuclear envelope dynamics and its loss causes microcephaly and diabetesDaphne J Smits, Rachel Schot, Nathalie Krusy, et al.
British Journal of Cancer|June 26, 2018
Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriersInge A P Derks-Smeets, Lieske H Schrijver, Christine E M de Die-Smulders, et al.
Cardiovascular and Interventional Radiology|September 3, 2024
The Paradox of Modern Technology in Standardizing Thermal Liver Ablation: Fostering Uniformity or Diversity?Coosje A M Verhagen, Ariadne L van der Velden, Reto Bale, et al.
Acta Obstetricia Et Gynecologica Scandinavica|November 19, 2016
Practice variation of vaginal birth after cesarean and the influence of risk factors at patient level: a retrospective cohort studyEmy Vankan, Ellen N Schoorel, Sander M van Kuijk, et al.
European Journal of Human Genetics : EJHG|March 31, 2025
DDX3X-related neurodevelopmental disorder in males - presenting a new cohort of 19 males and a literature reviewMilou G P Kennis, Dmitrijs Rots, Arjan Bouman, et al.
Annals of Surgery|February 22, 2023
Risk Models for Developing Pancreatic Fistula After Pancreatoduodenectomy: Validation in a Nationwide Prospective CohortThijs J Schouten, Anne Claire Henry, Francina J Smits, et al.
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