Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait-Reference-Cited by-同舟云学术

Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait

Published:2020-05-03 Issue:3 Volume:44 Page:211-213
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Sharma Praveen¹,Jandial Aditya²,Rajasekaran Sangamitra³,Das Reena¹^ORCID,Chhabra Sanjeev¹,Hira Jasbir Kaur¹,Khadwal Alka Rani²,Malhotra Pankaj²,Sharma Prashant¹^ORCID

Affiliation:

1. Departments of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh (Union Territory), India;

2. Department of Internal Medicine (Adult Clinical Hematology Division), Postgraduate Institute of Medical Education and Research, Chandigarh (Union Territory), India;

3. Pathology Group of Departments, Postgraduate Institute of Medical Education and Research, Chandigarh, (Union Territory), India

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1767128

Reference7 articles.

1. A novel double heterozygous, HbD Punjab/HbQ India, hemoglobinopathy

2. An Intriguing High Performance Liquid Chromatogram of a Double Heterozygosity for Hb Q-India/Hb D-Punjab

3. HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases

4. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

5. C-Window Peaks on CE-HPLC are Extremely Rare in Northern India, and Only Infrequently Represent HbC

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