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Pediatric Nephrology (Berlin, Germany)|December 3, 2013
The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1Anna Materna-Kiryluk, Krzysztof Kiryluk, Katelyn E Burgess, et al.
Children (Basel, Switzerland)|March 6, 2021
Maternal Risk Factors Associated with Limb Reduction Defects: Data from the Polish Registry of Congenital Malformations (PRCM)Anna Materna-Kiryluk, Katarzyna Wisniewska, Barbara Wieckowska, et al.
Nanomaterials (Basel, Switzerland)|May 12, 2026
Advanced Characterization of 2D Materials Using SLEEM/ToFVeronika Pizúrová, Jakub Piňos, Lukáš Průcha, et al.
The Review of Scientific Instruments|December 8, 2010
Improvement of the intrinsic time resolving power of the Cologne iron-free orange type electron spectrometersJ-M Régis, Th Materna, G Pascovici, et al.
Cardiology in the Young|August 31, 2021
Influence of fenestration on long-term Fontan survivalOndřej Materna, Vojtěch Illinger, Denisa Jičínská, et al.
Physical Review Letters|January 27, 2023
Origin of the Reactor Antineutrino Anomalies in Light of a New Summation Model with Parametrized β^{-} TransitionsA Letourneau, V Savu, D Lhuillier, et al.
Plos One|August 3, 2010
Unlocking short read sequencing for metagenomicsSébastien Rodrigue, Arne C Materna, Sonia C Timberlake, et al.
Frontiers in Genetics|December 2, 2020
Targeted Next-Generation Sequencing in the Diagnosis of Facial DysostosesEwelina Bukowska-Olech, Anna Materna-Kiryluk, Joanna Walczak-Sztulpa, et al.
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