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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 9, 2019
Correction to: Hybridization capture-based next-generation sequencing reliably detects FLT3 mutations and classifies FLT3-internal tandem duplication allelic ratio in acute myeloid leukemia: a comparative study to standard fragment analysisRong He, Daniel J Devine, Zheng Jin Tu, et al.
Mayo Clinic Proceedings|April 29, 1998
Hemoglobin Old Dominion/Burton-upon-Trent, beta 143 (H21) His-->Tyr, codon 143 CAC-->TAC--a variant with altered oxygen affinity that compromises measurement of glycated hemoglobin in diabetes mellitus: structure, function, and DNA sequenceG E Elder, T R Lappin, A B Horne, et al.
American Journal of Hematology|October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiencyPaola Bianchi, Elisa Fermo, Bertil Glader, et al.
American Journal of Clinical Pathology|May 12, 2021
Pathologic Spectrum and Molecular Landscape of Myeloid Disorders Harboring SF3B1 MutationsElise R Venable, Dong Chen, Constance P Chen, et al.
The Journal of Molecular Diagnostics : JMD|November 29, 2021
Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read SequencingAruna Rangan, Molly S Hein, William G Jenkinson, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
HGG Advances|February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1BJan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
British Journal of Pharmacology|February 18, 2014
The Concise Guide to PHARMACOLOGY 2013/14: overviewStephen P H Alexander, Helen E Benson, Elena Faccenda, et al.
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