Hemoglobin Shimonoseki HBA1:c.164A > G Illustrating the Continuing Utility of the Sickling Test and the Challenges in Antenatal Genetic Counselling
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-023-01670-1.pdf
Reference7 articles.
1. Sharma S, Sharma P, Das R, Chhabra S, Hira JK (2017) HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases. Ann Hematol 96:1227–1229
2. Das R, Ahluwalia J, Sachdeva MU (2016) Hematological practice in India. Hematol Oncol Clin North Am 30(2):433–444
3. Yamaoka K, Kawamura K, Hanada M et al (1960) Studies of abnormal hemoglobins. Jap J Hum Genet 5:99–111
4. Theodoridou S, Delaki E, Skatharoudi E, Karakasidou O, Vyzantiadis TA, Theodoridis T, Chalkia P (2018) First report of a coincidental discovery of Hb Shimonoseki [α54(E3)Gln→Arg, HBA2: c.164A > G (or HBA1)] in a greek family. Hemoglobin 42(4):281–282
5. Sharma P, Jandial A, Rajasekaran S, Das R, Chhabra S, Hira JK, Khadwal AR, Malhotra P, Sharma P (2020) Missing Hb Q-India peak in a triple-heterozygous patient with Hb D-Punjab/Hb Q-India/β-thalassemia trait. Hemoglobin 44(3):211–213
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1. Wide spectrum of novel and rare hemoglobin variants in the multi‐ethnic Indian population: A review;International Journal of Laboratory Hematology;2024-03-19
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