Citations (17)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (6)
Gui-Lan Chen, Lv-Yin Huang, Jian-Ying Zhou & Dong-Zhi Li. (2017) Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait. Hemoglobin 41:4-6, pages 291-292.
Read now
Read now
Giovanna Cardiero, Romeo Prezioso, Sabrina Dembech, Francesca Del Vecchio Blanco, Clelia Scarano & Giuseppina Lacerra. (2016) Identification and molecular characterization of a novel 163 kb deletion: The Italian (ϵγδβ)0-thalassemia. Hematology 21:5, pages 317-324.
Read now
Read now
Mohamed S. M. Khalil, Samy Marouf, David Element, Adele Timbs, Alice Gallienne, Anna Schuh, John M. Old & Shirley Henderson. (2014) A Study of δ-Globin Gene Mutations in the UK Population: Identification of Three Novel Variants and Development of a Novel DNA Test for Hb A′2. Hemoglobin 38:3, pages 201-206.
Read now
Read now
Imen Moumni, Amine Zorai, Sonia Mahjoub, Ikbel Mosbahi, Dorra Chaouechi, Neila Benromdhane & Salem Abbes. (2014) A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]. Hemoglobin 38:2, pages 88-90.
Read now
Read now
Attawut Chaibunruang, Goonnapa Fucharoen & Supan Fucharoen. (2012) First Description of a Hb A2 Variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai Individuals. Hemoglobin 36:1, pages 80-84.
Read now
Read now
Philippe Joly, Philippe Lacan, Caroline Garcia, Roland Meley, Corinne Pondarré & Alain Francina. (2011) A Novel Deletion/Insertion Caused by a Replication Error in the β-Globin Gene Locus Control Region. Hemoglobin 35:4, pages 316-322.
Read now
Read now
Articles from other publishers (11)
Serena Capasso, Giovanna Cardiero, Gennaro Musollino, Romeo Prezioso, Rosario Testa, Sabrina Dembech, Giulio Piluso, Vincenzo Nigro, F. Anna Digilio & Giuseppina Lacerra. (2023) Functional analysis of three new alpha-thalassemia deletions involving MCS-R2 reveals the presence of an additional enhancer element in the 5’ boundary region. PLOS Genetics 19:5, pages e1010727.
Crossref
Crossref
Giovanna Cardiero, Gennaro Musollino, Romeo Prezioso & Giuseppina Lacerra. (2021) mRNA Analysis of Frameshift Mutations with Stop Codon in the Last Exon: The Case of Hemoglobins Campania [α1 cod95 (−C)] and Sciacca [α1 cod109 (−C)]. Biomedicines 9:10, pages 1390.
Crossref
Crossref
Kritsada Singha, Goonnapa Fucharoen & Supan Fucharoen. (2021) δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia. Annals of Hematology 100:8, pages 1953-1963.
Crossref
Crossref
Stacy Colaco & Anita Nadkarni. (2021) Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers. Mutation Research/Reviews in Mutation Research 788, pages 108387.
Crossref
Crossref
Youqiong Li, Tongfeng Huang, Tian Mao, Xiuqun Zhang, Liang Liang & Menghui Meng. (2020)
Detection of a Hb A
2
‐Melbourne (HBD: c.130G>A) combined with β‐thalassemia in a Chinese individual
. Journal of Clinical Laboratory Analysis 34:9.
Crossref
Crossref
Giovanna Cardiero, Gennaro Musollino, Maria Grazia Friscia, Rosario Testa, Lucrezia Virruso, Caterina Di Girgenti, Mercedes Caldora, Rosario Colella Bisogno, Carlo Gaudiano, Giuseppe Manco & Giuseppina Lacerra. (2020) Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy. Genes 11:8, pages 870.
Crossref
Crossref
F. Sinem Hocaoglu-Emre, Guven Yenmis, Devrim Saribal & Cengiz Yakicier. (2019) IVSII-74 T>G: As harmless as we thought?. Turkish Journal of Biochemistry 44:1, pages 41-46.
Crossref
Crossref
H. Wajcman, M. Azimi, J. Cui, C. Hoppe, M. Flamini, C. Ho & S. Reddy. (2016)
Hemoglobinopathy testing: the significance of accuracy and pitfalls in HbA
2
determination
. International Journal of Laboratory Hematology 39:1.
Crossref
Crossref
Maria Luisa González Borrachero, Félix de la Fuente-Gonzalo, Fernando Ataúlfo González, Jorge M. Nieto, Ana Villegas & Paloma Ropero. (2015) Delta0-talasemia por inserción de 27 pares de bases en el gen δ-globina con descenso de los valores de hemoglobina A2. Medicina Clínica 144:7, pages 312-316.
Crossref
Crossref
Maria Luisa González Borrachero, Félix de la Fuente-Gonzalo, Fernando Ataúlfo González, Jorge M. Nieto, Ana Villegas & Paloma Ropero. (2015) Delta0-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A2 levels. Medicina Clínica (English Edition) 144:7, pages 312-316.
Crossref
Crossref
Sitthichai Panyasai, Goonnapa Fucharoen & Supan Fucharoen. (2015) Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening. Clinica Chimica Acta 438, pages 226-230.
Crossref
Crossref