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British Journal of Haematology|November 17, 2006
Cell-free DNA levels in pregnancies at risk of sickle-cell disease and significant ethnic variationAgeliki Gerovassili, Kypros H Nicolaides, Swee Lay Thein, et al.
Bio-Protocol|March 18, 2021
An Imaging Flow Cytometry Method to Measure Citrullination of H4 Histone as a Read-out for Neutrophil Extracellular Traps FormationEmilia A Barbu, Venina M Dominical, Laurel Mendelsohn, et al.
Blood Advances|March 10, 2022
Genetic variants of PKLR are associated with acute pain in sickle cell diseaseXunde Wang, Kate Gardner, Mickias B Tegegn, et al.
British Journal of Haematology|October 9, 2003
Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia traitChad Garner, Tracy K Dew, Roy Sherwood, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 27, 2016
Alpha-thalassaemia trait as a cause of unexplained microcytosis in a South African populationSakina Bibi Loonat, Nitien Hira Naran, Swee Lay Thein, et al.
American Journal of Human Genetics|February 1, 2002
Evidence of genetic interaction between the beta-globin complex and chromosome 8q in the expression of fetal hemoglobinChad P Garner, Thanusak Tatu, Steve Best, et al.
British Journal of Haematology|October 10, 2012
HbA2 levels in normal adults are influenced by two distinct genetic mechanismsStephan Menzel, Chad Garner, Helen Rooks, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3Nancy F Hansen, Xunde Wang, Mickias B Tegegn, et al.
British Journal of Haematology|September 27, 2003
A novel deletion causing (epsilon gamma delta beta) degrees thalassaemia in a Chilean familyLaurence Game, Jean Bergounioux, James Paul Close, et al.
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