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27 results on '"Yeager, Meredith"'

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1. Increased Frequency of Mosaic Chromosomal Alterations in Peripheral Blood Samples of Sub-Saharan African Children with Endemic Burkitt Lymphoma

2. Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study

3. HBB rs334, ABO R s8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

4. Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families

5. HBB rs334, ABO Rs8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

6. Germline-Somatic Interactions in Myelofibrosis Susceptibility

9. Pre-Transplant Clonal Mosaicism Is Associated with Increased Relapse and Lower Survival in Acute Lymphoblastic Leukemia Patients Undergoing Allogeneic Hematopoietic Cell Transplant

10. Chromosomal Aberrations in Pre-HCT Blood Samples and Outcomes after Transplantation in Patients with Myelofibrosis

11. Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia

12. De Novo and Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome: Similarities and Differences in SNP-Array Detected Chromosomal Aberrations in Pre-Transplant Blood Samples

13. HBB rs334, ABO Rs8176703and Plasmodium FalciparumPositivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

14. Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

15. Germline Mutations in Patients Receiving Unrelated Donor Hematopoietic Cell Transplant for Severe Aplastic Anemia

16. Novel and Known Ribosomal Causes of Diamond-Blackfan Anemia Identified through Comprehensive Genomic Characterization

18. Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies

19. Functional Consequences Of RPS29 Germline Mutations In Diamond-Blackfan Anemia

20. RPS29 is Mutated in a Multi-Case Diamond Blackfan Anemia Family

21. Germline Mutations in RTEL1 cause Dyskeratosis Congenita

22. Whole-exome sequencing and functional studies identify RPS29as a novel gene mutated in multicase Diamond-Blackfan anemia families

23. Whole exome sequencing in families with CLL detects a variant in Integrin β 2associated with disease susceptibility

24. De Novoand Therapy-Related Acute Myeloid Leukemia and Myelodysplastic Syndrome: Similarities and Differences in SNP-Array Detected Chromosomal Aberrations in Pre-Transplant Blood Samples

25. Functional Consequences Of RPS29Germline Mutations In Diamond-Blackfan Anemia

26. Germline Mutations in RTEL1cause Dyskeratosis Congenita

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