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Your search keyword '"Okoli, Steven"' showing total 16 results

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1. Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

2. GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

3. Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level

4. Whole-genome sequencing of patients with rare diseases in a national health system

5. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

6. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

7. Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

8. Recapitulation of erythropoiesis in congenital dyserythropoietic anemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities

9. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

11. Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I)

12. A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

14. Emerging treatments for essential thrombocythemia

15. Emerging treatments for essential thrombocythemia.

16. Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

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