Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 31, 2002
Central nervous system embryogenesis and its failuresFelicitas L Lacbawan, Maximilian Muenke
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2014
Molecular testing for the BRCA1 and BRCA2 Ashkenazi Jewish founder mutations: a report on the College of American Pathologists proficiency testing surveysLaura J Tafe, Michael B Datto, Glenn E Palomaki, et al.
Archives of Pathology & Laboratory Medicine|January 3, 2012
Verification of performance specifications of a molecular test: cystic fibrosis carrier testing using the Luminex liquid bead arrayFelicitas L Lacbawan, Karen E Weck, Jeffrey A Kant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2013
Three-year experience of a CAP/ACMG methods-based external proficiency testing program for laboratories offering DNA sequencing for rare inherited disordersC Sue Richards, Glenn E Palomaki, Felicitas L Lacbawan, et al.
The Journal of Molecular Diagnostics : JMD|March 4, 2015
Improving Molecular Genetic Test Utilization through Order Restriction, Test Review, and GuidanceJacquelyn D Riley, Gary W Procop, Kandice Kottke-Marchant, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 1, 2024
Biotinidase biochemical and molecular analyses: Experience at a large reference laboratoryRajesh Sharma, Cathlin R Kucera, Camille R Nery, et al.
Molecular Genetics & Genomic Medicine|February 2, 2019
Prenatal cell-free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratoryCarrie Guy, Farnoosh Haji-Sheikhi, Charles M Rowland, et al.
Blood Cancer Journal|April 23, 2023
NGS-defined measurable residual disease (MRD) after initial chemotherapy as a prognostic biomarker for acute myeloid leukemiaYonghong Li, Jose Solis-Ruiz, Fei Yang, et al.
Molecular Genetics and Metabolism Reports|March 18, 2021
Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemiaYue Huang, Rajesh Sharma, Annette Feigenbaum, et al.
Human Mutation|May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutationsAileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
Pageof 2