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Ekaterina Demidova, Valentina Salomashkina, Daria Selivanova, Evgeny Litvin, Natalia Karamyan, Svetlana Mann, Valentina Dvirnyk, Salia Maryina, Natal’ya Petrova, Lana Gorgidze, Anastasiya Peredel’skaya, Nina Tsvetaeva, Nataliya Smetanina & Vadim Surin. (2023) Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25. Hemoglobin 47:2, pages 97-101.
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Manit Nuinoon, Orapan Thipthara & Suthat Fucharoen. (2019) Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2. Hemoglobin 43:1, pages 52-55.
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Jiajie Pu, Li Zhang, Xiaofeng Wei & Xiangmin Xu. (2018) Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual. Hemoglobin 42:3, pages 184-188.
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Antonio Amato, Maria Pia Cappabianca, Maria Perri, Ivo Zaghis, Fabrizio Mastropietro, Donatella Ponzini, Paola Di Biagio & Roberta Piscitelli. (2012) Hb Filottrano [codon 120 (–A)]: A Novel Frameshift Mutation in Exon 3 of the β-Globin Gene Causing Dominantly Inherited β-Thalassemia Intermedia. Hemoglobin 36:5, pages 480-484.
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Pierre Chagnon, Luigina Mollica, Claude Belisle, Céline Deveaux, Giovanni D. Angelo, Denis-Claude Roy, Denis Soulières & Lambert Busque. (2008) Hb Montreal II: A Novel Elongated β-Globin Variant Caused by a Frameshift Mutation [β142 (−C)]. Hemoglobin 32:4, pages 351-359.
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Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina. (2007) Two New β0-Thalassemic Mutations: A Deletion (−CC) at Codon 142 or Overlapping Codons 142-143, and an Insertion (+T) at Codon 45 or Overlapping Codons 44-45/45-46 of the β-Globin Gene. Hemoglobin 31:2, pages 159-165.
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Claude Préhu, Serge Pissard, Maha Al-Sheikh, Catherine Le Niger, Dora Bachir, Fréderic Galactéros & Henri Wajcman. (2005) Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [CAG→TAG (Gln→Stop]). Hemoglobin 29:3, pages 229-233.
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Articles from other publishers (1)
B.I. Weinstein, B. Erramouspe, D.M. Albuquerque, D.M. Oliveira, E.M. Kimura, F.F. Costa & M.F. Sonati. (2006) Hb Florida: A novel elongated C‐terminal β‐globin variant causing dominant β‐thalassemia phenotype. American Journal of Hematology 81:5, pages 358-360.
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