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Hemoglobin

Showing results (781-790 of 2,379) with videos related to

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Hemoglobin|June 29, 2012
Identification of a new HBA1 gene mutation (HBA1:c.301-2A>T) in cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser]Karen G Scheps, Amanda Binaghi, Viviana Varela
Hemoglobin|June 29, 2012
A new Frameshift mutation on the α2-globin gene causing α⁺-thalassemia: codon 43 (TTC>-TC or TTC>T-C)Philippe Joly, Philippe Lacan, Caroline Garcia, et al.
Hemoglobin|July 17, 2012
A 25-year observation of a Japanese female patient with Hb Nottingham who has two children with the same disorderYuko Cho, Susumu Iizuka, Yoshio Hatae, et al.
Hemoglobin|January 1, 1979
Globin chain synthesis in beta-thalassemia with normal hemoglobins A2 and FM Aksoy, G Almiş, E Bermek
Hemoglobin|January 1, 1979
Hemoglobin Suan-Dok (alpha 2 109 (G16) Leu replaced by Arg beta 2): an unstable variant associated with alpha-thalassemiaT Sanguansermsri, S Matragoon, L Changloah, et al.
Hemoglobin|January 1, 1979
Application of an automatic oxygenation technique to analysis of oxygen equilibrium curves for hemoglobinopathic red cells and functional screening of clinically important hemoglobinopathiesA Hayashi, K Kidoguchi, T Suzuki, et al.
Hemoglobin|January 1, 1979
Immunologic diagnosis of alpha-thalassemia traitsP Wasi, P Pravatmuang, P Winichagoon
Hemoglobin|January 1, 1990
An initiation codon mutation as a cause of a beta-thalassemiaL Jankovic, G D Efremov, O Josifovska, et al.
Hemoglobin|June 28, 2012
Low fixed-dose hydroxyurea in severely affected Indian children with sickle cell diseaseDipty L Jain, Vijaya Sarathi, Saumil Desai, et al.
Hemoglobin|September 8, 1998
Hb Oita [alpha45(CE3)His-->Pro]: a new silent hemoglobin variantK Hamaguchi, K Harano, T Harano, et al.
Pageof 238

Showing results (781-790 of 2,379) with videos related to

Sort By:
Pageof 238
Hemoglobin|June 29, 2012
Identification of a new HBA1 gene mutation (HBA1:c.301-2A>T) in cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser]Karen G Scheps, Amanda Binaghi, Viviana Varela
Hemoglobin|June 29, 2012
A new Frameshift mutation on the α2-globin gene causing α⁺-thalassemia: codon 43 (TTC>-TC or TTC>T-C)Philippe Joly, Philippe Lacan, Caroline Garcia, et al.
Hemoglobin|July 17, 2012
A 25-year observation of a Japanese female patient with Hb Nottingham who has two children with the same disorderYuko Cho, Susumu Iizuka, Yoshio Hatae, et al.
Hemoglobin|January 1, 1979
Globin chain synthesis in beta-thalassemia with normal hemoglobins A2 and FM Aksoy, G Almiş, E Bermek
Hemoglobin|January 1, 1979
Hemoglobin Suan-Dok (alpha 2 109 (G16) Leu replaced by Arg beta 2): an unstable variant associated with alpha-thalassemiaT Sanguansermsri, S Matragoon, L Changloah, et al.
Hemoglobin|January 1, 1979
Application of an automatic oxygenation technique to analysis of oxygen equilibrium curves for hemoglobinopathic red cells and functional screening of clinically important hemoglobinopathiesA Hayashi, K Kidoguchi, T Suzuki, et al.
Hemoglobin|January 1, 1979
Immunologic diagnosis of alpha-thalassemia traitsP Wasi, P Pravatmuang, P Winichagoon
Hemoglobin|January 1, 1990
An initiation codon mutation as a cause of a beta-thalassemiaL Jankovic, G D Efremov, O Josifovska, et al.
Hemoglobin|June 28, 2012
Low fixed-dose hydroxyurea in severely affected Indian children with sickle cell diseaseDipty L Jain, Vijaya Sarathi, Saumil Desai, et al.
Hemoglobin|September 8, 1998
Hb Oita [alpha45(CE3)His-->Pro]: a new silent hemoglobin variantK Hamaguchi, K Harano, T Harano, et al.
Pageof 238