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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 2
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Short Communication

Coinheritance of Hb D-Punjab and β-Thalassemia: Diagnosis and Implications in Prenatal Diagnosis

Sheila DasDepartment of Pathology, Christian Medical College, Ludhiana, Punjab, India and
&
Ranjeet S. MashonDepartment of Haematopathology, Christian Medical College, Ludhiana, Punjab, IndiaCorrespondence[email protected]
Pages 138-140 | Received 22 Jul 2014, Accepted 28 Aug 2014, Published online: 10 Feb 2015

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Adriaan J. van Gammeren, Leonie Pelkmans, Corné C.W. van Endschot, Roseri J.A.C. Roelofsen-de Beer & Cornelis L. Harteveld. (2020) An Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C). Hemoglobin 44:1, pages 61-63.
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Articles from other publishers (9)

Anamul Hasan, Jigishu Ahmed, Bikash Chandra Chanda, Maisha Aniqua, Raisa Akther, Palash Kanti Dhar, Kazi Afrin Binta Hasan, Abdur Rouf Siddique, Md. Zahidul Islam, Sharmine Zaman Urmee & Dinesh Mondal. (2023) Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr,b in Bangladesh. Thalassemia Reports 13:2, pages 131-143.
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Vineeta Gupta & Priyanka Aggarwal. (2023) Mandatory Testing for Hemoglobinopathies: Need of the Hour!. Indian Pediatrics 60:4, pages 322-322.
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Neha Singh, Tulika Seth & Seema Tyagi. (2023) Review of clinical and hematological profile of hemoglobin D cases in a single centre. Journal of Marine Medical Society 25:3, pages 74.
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Vineeta Gupta & Priyanka Aggarwal. (2022) Profile of Hemoglobin D (HbD) Disease in Eastern Uttar Pradesh: A Single-Center Experience. Cureus.
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Srdjan Denic & Abdul-Kader Souid. (2021) Hemoglobin D-Punjab Homozygotes and Double Heterozygotes in Premarital Screening: Case Presentations and Minireview. European Journal of Medical and Health Sciences 3:1, pages 90-94.
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Barbara J. Bain. 2020. Haemoglobinopathy Diagnosis. Haemoglobinopathy Diagnosis 261 324 .
A A PETRENKO, A V PIVNIK, P P KIM, E Yu DEMIDOVA, V L SURIN, A O ABDULLAEV, A B SUDARIKOV, N A PETROVA & S A MARYINA. (2018) Coinheritance of HbD-Punjab/β+-thalassemia (IVSI+5 G-C) in patient with Gilbert's syndrome. Terapevticheskii arkhiv 90:7, pages 105-109.
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Sitthichai Panyasai, Supachai Sakkhachornphop & Sakorn Pornprasert. (2017) Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA2 Levels on Capillary Electrophoresis. Indian Journal of Hematology and Blood Transfusion 34:1, pages 110-114.
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Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2016) Analysis of the population genetic structure of Hb D-Los Angeles [β121 (GH4) Glu→Gln G AA→ C AA] in Denizli, Turkey; genetic diversity, historical demography and estimation of the mutation rates based on haplotype variation . American Journal of Human Biology 28:4, pages 476-483.
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