C. Wei

发表

Mixed fields on RhD typing as an indication of loss of heterozygosity on chromosome 1p in acute myeloid leukemia

S. Kamel‐Reid, K. Craddock, Vikas Gupta, 2015, Leukemia & lymphoma.

Genetic determinants of extracellular magnesium concentration: analysis of multiple candidate genes, and evidence for association with the estrogen receptor alpha (ESR1) locus.

D. Cole, A. Shuen, C. Wei, 2009, Clinica chimica acta; international journal of clinical chemistry.

Monitoring of Minimal Residual Hematologic Disease

S. Kamel‐Reid, J. Lipton, C. Wei, 2009 .

Special Article Inter-Laboratory Comparison of Chronic Myeloid Leukemia Minimal Residual Disease Monitoring Summary and Recommendations

S. Kamel‐Reid, Tong Zhang, J. Lipton, 2007 .

Measurable residual disease monitoring provides insufficient lead-time to prevent morphological relapse in the majority of patients with core-binding factor acute myeloid leukemia

M. Minden, Steven M. Chan, S. Kamel‐Reid, 2020, Haematologica.

Sample Features Associated with Success Rates in Population-Based EGFR Mutation Testing

M. Tsao, G. da Cunha Santos, S. Kamel‐Reid, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Upfront Next Generation Sequencing in Non-Small Cell Lung Cancer

M. Tsao, F. Shepherd, C. Cheung, 2022, Current oncology.

Overexpression of asparagine synthetase in albizziin-resistant murine diploid embryonic stem cells

I. Andrulis, C. Wei, C. Wei, 1993, Somatic cell and molecular genetics.

Lung transplantation complicated by graft‐versus‐host disease and confounded by incidental transfusion‐associated macrochimerism

S. Kamel‐Reid, K. Pavenski, C. Cserti-Gazdewich, 2008, Transfusion.

Inter-laboratory comparison of chronic myeloid leukemia minimal residual disease monitoring: summary and recommendations.

Suzanne Kamel-Reid, S. Kamel‐Reid, Tong Zhang, 2007, The Journal of molecular diagnostics : JMD.

Recurrent familial hypocalcemia due to germline mosaicism for an activating mutation of the calcium-sensing receptor gene.

G. Hendy, D. Cole, L. Canaff, 2003, The Journal of clinical endocrinology and metabolism.

Radar plots facilitate differential diagnosis of acute promyelocytic leukemia and NPM1+ acute myeloid leukemia by flow cytometry

A. Porwit, J. Mazur, E. Hyjek, 2020, Cytometry. Part B, Clinical cytometry.

Primary Marginal Zone Lymphoma of the Subcutis Associated With Panniculitis and Fat Necrosis.

J. Delabie, V. Kukreti, C. Wei, 2015, American journal of clinical pathology.

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

R. Weksberg, J. Squire, P. Ray, 2001, Human molecular genetics.