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Hemoglobin|October 23, 2013
Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobinSarmad Toma, María Tenorio, Matthew Oakley, 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.Current Opinion in Hematology|July 6, 2010
The role of thromboprophylaxis in cancer patients: emerging dataLaurel A Menapace, Alok A KhoranaBritish 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.BMC Genomics|June 1, 2004
Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adultsJames Close, Laurence Game, Barnaby Clark, et al.Hemoglobin|June 17, 2017
Detection of Hb Rothschild HBB: c.[112T>A or 112T>C], Through High Index of Suspicion on Abnormal Pulse OximetryNazeer A Alli, Piet Wessels, Narisha Rampersad, et al.Thorax|December 1, 2017
Heterogeneity of respiratory disease in children and young adults with sickle cell diseaseAlan Lunt, Lucy Mortimer, David Rees, et al.Prenatal Diagnosis|December 8, 2006
Free fetal DNA in maternal circulation: a potential prognostic marker for chromosomal abnormalities?Ageliki Gerovassili, Chad Garner, Kypros H Nicolaides, et al.Pageof 18