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Showing results (81-90 of 3,216) with videos related to
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Hemoglobin
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November 23, 2017
Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α<sup>0</sup>-Thalassemia in a Chinese Family
Sheng He, Qian Qin, Peng Huang, et al.
Hemoglobin
|
September 28, 2017
Rivaroxaban Use in Patients with Hemoglobinopathies
Chrysoula Apostolou, Philippos Klonizakis, Maria Mainou, et al.
Hemoglobin
|
January 8, 2019
First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family
Sheng He, Qian Qin, Li Lin, et al.
Hemoglobin
|
January 11, 2019
Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical Implications
Aikaterini Zioga, Eleni Thanopoulou, Elissavet Hatzi, et al.
Hemoglobin
|
January 11, 2019
Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India
Ajit C Gorakshakar, Pearl V Breganza, Stacy P Colaco, et al.
Hemoglobin
|
March 17, 2007
Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation
Imen Moumni, Amine Zorai, Bechir Ben Daoued, et al.
Hemoglobin
|
March 17, 2007
Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child
Dongzhi Li, Can Liao, Jian Li
Hemoglobin
|
January 1, 1990
Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes
S Agarwal, R Oner, F Kutlar, et al.
Hemoglobin
|
January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expression
S Abbes, S Fattoum, M Vidaud, et al.
Hemoglobin
|
January 1, 1991
Pneumococcal septicemia and meningitis in an infant with Hb S/D-Los Angeles disease: a failure of neonatal hemoglobinopathy screening
S H Abhyankar, S T Miller, S P Rao, et al.
Page
of 322
Search research articles
Search
Showing results (81-90 of 3,216) with videos related to
Sort By:
Page
of 322
Hemoglobin
|
November 23, 2017
Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α<sup>0</sup>-Thalassemia in a Chinese Family
Sheng He, Qian Qin, Peng Huang, et al.
Hemoglobin
|
September 28, 2017
Rivaroxaban Use in Patients with Hemoglobinopathies
Chrysoula Apostolou, Philippos Klonizakis, Maria Mainou, et al.
Hemoglobin
|
January 8, 2019
First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family
Sheng He, Qian Qin, Li Lin, et al.
Hemoglobin
|
January 11, 2019
Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical Implications
Aikaterini Zioga, Eleni Thanopoulou, Elissavet Hatzi, et al.
Hemoglobin
|
January 11, 2019
Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India
Ajit C Gorakshakar, Pearl V Breganza, Stacy P Colaco, et al.
Hemoglobin
|
March 17, 2007
Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation
Imen Moumni, Amine Zorai, Bechir Ben Daoued, et al.
Hemoglobin
|
March 17, 2007
Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child
Dongzhi Li, Can Liao, Jian Li
Hemoglobin
|
January 1, 1990
Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes
S Agarwal, R Oner, F Kutlar, et al.
Hemoglobin
|
January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expression
S Abbes, S Fattoum, M Vidaud, et al.
Hemoglobin
|
January 1, 1991
Pneumococcal septicemia and meningitis in an infant with Hb S/D-Los Angeles disease: a failure of neonatal hemoglobinopathy screening
S H Abhyankar, S T Miller, S P Rao, et al.
Page
of 322