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Hemoglobin|August 1, 1996
Sickle cell gene in the population of Saudi ArabiaM A el-Hazmi, A S Warsy, A R al-Swailem, et al.Hemoglobin|November 1, 1996
A Dutch family with Hb Atlanta [beta 75(E19)Leu-->Pro]V Aygün, R van Zwieten, C J Pronk-Admiraal, et al.Hemoglobin|November 1, 1996
Hb Cook [beta 132(H10)Lys-->Thr]: a new hemoglobin variant in a southeast Asian familyP J Hutt, V F Fairbanks, T C Griffin, et al.Hemoglobin|November 1, 1996
Partial splenectomy in children with sickle cell disease and repeated episodes of splenic sequestrationE Svarch, P Vilorio, I Nordet, et al.Hemoglobin|November 1, 1996
The gamma-globin gene rearrangements in newborns from the Republic of MacedoniaG D Efremov, A J Dimovski, Z Popovski, et al.Hemoglobin|January 1, 1977
Structure in relation to behavior of mutant hemoglobins in citrate agar electrophoresisR G Schneider, B HightowerHemoglobin|May 16, 2015
A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H DiseaseSamaneh Farashi, Negin Faramarzi Garous, Fatemeh Zeinali, et al.Hemoglobin|May 16, 2015
Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the QuestionSule Unal, David H K Chui, Fatma GumrukHemoglobin|November 17, 2010
Hb Sarrebourg [β131(H9)Gln→Arg, CAG>CGG] in TurkeyM Akif Cürük, Aydan Ç Cavusoglu, Huriye Arıcan, et al.Hemoglobin|November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chainLoïc Garçon, Achille Iolascon, Serge Pissard, et al.Pageof 240