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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: May 08, 2024
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Identifying patients at risk for hereditary myeloid malignancy syndromes incorporating a novel, self-administered questionnaire to an initial screening platform.
Mohammad Faizan Zahid et al. Eur J Haematol 2023
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ASSESSING PATIENT ATTITUDES TOWARD GENETIC TESTING FOR HEREDITARY HEMATOLOGIC MALIGNANCY.
Johnson Addison Q et al. European journal of haematology 2022
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Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes.
McReynolds Lisa J et al. Blood 2022
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The predictive value of PNH clones, 6p CN-LOH, and clonal TCR gene rearrangement for aplastic anemia diagnosis.
Shah Yash B et al. Blood advances 2021 5(16) 3216-3226
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Local Coverage Determination (LCD): Flow Cytometry (L33661)
The U.S. Centers for Medicare & Medicaid Services
The diagnostic utility of targeted gene panel sequencing in discriminating etiologies of cytopenia.
Zheng Gang et al. American journal of hematology 2019 Jul
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Clinical applicability of proposed algorithm for identifying individuals at risk for hereditary hematologic malignancies.
Clifford Maggie et al. Leukemia & lymphoma 2019 Jul 1-8
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Acquired and germline predisposition to bone marrow failure: Diagnostic features and clinical implications.
Kallen Michael E et al. Seminars in hematology 2019 56(1) 69-82
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Old and new tools in the clinical diagnosis of inherited bone marrow failure syndromes.
West Allison H et al. Hematology. American Society of Hematology. Education Program 2017 2017(1) 79-87
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Clinical implications of somatic mutations in aplastic anemia and myelodysplastic syndrome in genomic age.
Maciejewski Jaroslaw P et al. Hematology. American Society of Hematology. Education Program 2017 2017(1) 66-72
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 08, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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