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Tatiana Tvrdik

Showing results (1-10 of 19) with videos related to

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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 21, 2024
Genomic Insights Into High-Grade Infarct-Associated Bone SarcomasTatiana Tvrdik, Sandra Gjorgova Gjeorgjievski, Philip Wong, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testingChristine E Miller, Patti Krautscheid, Erin E Baldwin, et al.
American Journal of Medical Genetics. Part A|March 11, 2015
Stress and coping in parents of children with Prader-Willi syndrome: Assessment of the impact of a structured plan of careTatiana Tvrdik, Debbie Mason, Karin M Dent, et al.
Transfusion|November 25, 2022
Loss of heterozygosity leading to incorrect HLA typing for platelet-transfusion refractory patientMichael Horwath, Tatiana Tvrdik, Debra Saxe, et al.
Clinical Case Reports|December 20, 2018
Novel mutation in <i>CCBE 1</i> as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1Dora J Melber, Tara S Andreasen, Rong Mao, et al.
Human Mutation|February 24, 2017
Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz SyndromeColleen M Carlston, Anne H O'Donnell-Luria, Hunter R Underhill, et al.
The Journal of Molecular Diagnostics : JMD|October 20, 2022
Clinical Validation and Diagnostic Utility of Optical Genome Mapping for Enhanced Cytogenomic Analysis of Hematological NeoplasmsNikhil S Sahajpal, Ashis K Mondal, Tatiana Tvrdik, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
A rapid gene sequencing panel strategy to facilitate precision neonatal medicineLuca Brunelli, Rong Mao, Sabrina Malone Jenkins, et al.
NPJ Genomic Medicine|July 16, 2021
Effective variant filtering and expected candidate variant yield in studies of rare human diseaseBrent S Pedersen, Joe M Brown, Harriet Dashnow, et al.
Pediatric Research|February 4, 2022
Evaluating use of changing technologies for rapid next-generation sequencing in pediatricsRachel Palmquist, Sabrina Malone Jenkins, Dawn Bentley, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 21, 2024
Genomic Insights Into High-Grade Infarct-Associated Bone SarcomasTatiana Tvrdik, Sandra Gjorgova Gjeorgjievski, Philip Wong, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testingChristine E Miller, Patti Krautscheid, Erin E Baldwin, et al.
American Journal of Medical Genetics. Part A|March 11, 2015
Stress and coping in parents of children with Prader-Willi syndrome: Assessment of the impact of a structured plan of careTatiana Tvrdik, Debbie Mason, Karin M Dent, et al.
Transfusion|November 25, 2022
Loss of heterozygosity leading to incorrect HLA typing for platelet-transfusion refractory patientMichael Horwath, Tatiana Tvrdik, Debra Saxe, et al.
Clinical Case Reports|December 20, 2018
Novel mutation in <i>CCBE 1</i> as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia-lymphedema syndrome-1Dora J Melber, Tara S Andreasen, Rong Mao, et al.
Human Mutation|February 24, 2017
Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz SyndromeColleen M Carlston, Anne H O'Donnell-Luria, Hunter R Underhill, et al.
The Journal of Molecular Diagnostics : JMD|October 20, 2022
Clinical Validation and Diagnostic Utility of Optical Genome Mapping for Enhanced Cytogenomic Analysis of Hematological NeoplasmsNikhil S Sahajpal, Ashis K Mondal, Tatiana Tvrdik, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
A rapid gene sequencing panel strategy to facilitate precision neonatal medicineLuca Brunelli, Rong Mao, Sabrina Malone Jenkins, et al.
NPJ Genomic Medicine|July 16, 2021
Effective variant filtering and expected candidate variant yield in studies of rare human diseaseBrent S Pedersen, Joe M Brown, Harriet Dashnow, et al.
Pediatric Research|February 4, 2022
Evaluating use of changing technologies for rapid next-generation sequencing in pediatricsRachel Palmquist, Sabrina Malone Jenkins, Dawn Bentley, et al.
Pageof 2