Hb Memphis [HBA2: c.70G>C (orHBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C)-Reference-Cited by-同舟云学术

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Hb Memphis [HBA2: c.70G>C (orHBA1)] in a Turkish Child: A Case Report and Comparison to Hb Q-Thailand (HBA1: c.223G>C)

Published:2014-01-16 Issue:2 Volume:38 Page:137-141
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Lubrano Lauren,Donnelly Michael J.,Sandler Gerald,Hoyer James D.,Swanson Kenneth C.,Dawson D. Brian,Oliveira Jennifer L.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.867866

Reference9 articles.

1. The diagnostic dilemma of congenital unstable hemoglobinopathies

2. Characterization of α23GluNH2in Hemoglobin Memphis. Hemoglobin Memphis/S, a New Variant of Molecular Disease*

3. Sickle Cell Anemia with Two Adult Hemoglobins—Hb S and Hb GPhiladelphia/S

4. Homozygous Sickle-cell Anaemia Arising from two Different Haemoglobins S

5. A third case of hemoglobin memphis/sickle cell disease

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2. Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing;The Journal of Molecular Diagnostics;2021-12

3. Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M‐hemoglobin variants;International Journal of Laboratory Hematology;2021-06-06

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