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Showing results (431-440 of 3,216) with videos related to
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Hemoglobin
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December 19, 2018
The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature
Karen G Scheps, Viviana Varela, Héctor M Targovnik
Hemoglobin
|
January 5, 2020
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran
Zahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, et al.
Hemoglobin
|
January 25, 2020
An Unusual Compound Heterozygosity for Hb O-Arab (<i>HBB</i>: c.364G>A) and Hb D-Los Angeles (<i>HBB</i>: c.364G>C)
Adriaan J van Gammeren, Leonie Pelkmans, Corné C W van Endschot, et al.
Hemoglobin
|
October 29, 2019
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG<i>T</i>>AG<i>G</i>); <i>HBB</i>: c.270T>G] Resulting in Hemoglobin Vanderbilt
William Shomali, Rondeep Brar, Subramanyeswara R Arekapudi, et al.
Hemoglobin
|
January 1, 1992
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patient
F F Costa, M S Figueredo, M F Sonati, et al.
Hemoglobin
|
January 1, 1992
Hemoglobinopathies in Yugoslavia: an update
G D Efremov
Hemoglobin
|
January 1, 1992
Mild Hb Constant Spring-Hb H disease with beta zero-thalassemia trait
X J Wen, S Liang
Hemoglobin
|
January 1, 1992
Hemoglobinopathies in Sardinia
B Masala
Hemoglobin
|
June 1, 2005
Molecular and clinical features of Hb H disease in northern Thailand
Pimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, et al.
Hemoglobin
|
June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16
Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.
Page
of 322
Search research articles
Search
Showing results (431-440 of 3,216) with videos related to
Sort By:
Page
of 322
Hemoglobin
|
December 19, 2018
The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature
Karen G Scheps, Viviana Varela, Héctor M Targovnik
Hemoglobin
|
January 5, 2020
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran
Zahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, et al.
Hemoglobin
|
January 25, 2020
An Unusual Compound Heterozygosity for Hb O-Arab (<i>HBB</i>: c.364G>A) and Hb D-Los Angeles (<i>HBB</i>: c.364G>C)
Adriaan J van Gammeren, Leonie Pelkmans, Corné C W van Endschot, et al.
Hemoglobin
|
October 29, 2019
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG<i>T</i>>AG<i>G</i>); <i>HBB</i>: c.270T>G] Resulting in Hemoglobin Vanderbilt
William Shomali, Rondeep Brar, Subramanyeswara R Arekapudi, et al.
Hemoglobin
|
January 1, 1992
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patient
F F Costa, M S Figueredo, M F Sonati, et al.
Hemoglobin
|
January 1, 1992
Hemoglobinopathies in Yugoslavia: an update
G D Efremov
Hemoglobin
|
January 1, 1992
Mild Hb Constant Spring-Hb H disease with beta zero-thalassemia trait
X J Wen, S Liang
Hemoglobin
|
January 1, 1992
Hemoglobinopathies in Sardinia
B Masala
Hemoglobin
|
June 1, 2005
Molecular and clinical features of Hb H disease in northern Thailand
Pimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, et al.
Hemoglobin
|
June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16
Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.
Page
of 322