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Hemoglobin
international journal for hemoglobin research
Volume 15, 1991 - Issue 5
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Original Article

Six Rare Hemoglobin Variants Found in Sicily

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Pages 431-437 | Received 18 Jan 1991, Accepted 27 Jun 1991, Published online: 07 Jul 2009

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Read on this site (6)

Georgi Petkov, Marija Dimishkovska, Vanya Tsoneva Ivanova, Georgi Yordanov, Alexandar Zdraveski & Dijana Plaseska-Karanfilska. (2015) Hb G-Waimanalo [A1] or α64(E13)Asp→Asn (α1) (HBA1: c.193G>A) Observed in a Bulgarian Family. Hemoglobin 39:6, pages 430-431.
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Mohammad Reza Mahdavi, Mehran Karimi, Majid Yavarian, Payam Roshan, Mehrnoush Kosaryan & Rita Siami. (2011) Detection of Hb Setif in North Iran and the Question of Its Origin: Iranian or Multiethnic?. Hemoglobin 35:2, pages 152-156.
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Marianthi Georgitsi, Adamantia Papachatzopoulou, Emmanouella Linardaki, Vassilis Maroulis, Manoussos N. Papadakis & George P. Patrinos. (2011) First Report of Hb A2-NYU (HBD:c.39T>A) in the Hellenic Population. Hemoglobin 35:1, pages 91-95.
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Phannee Sawangareetrakul, Saovaros Svasti, Boonpa Yodsowon, Pranee Winichagoon, Chantragan Srisomsap, Jisnuson Svasti & Suthat Fucharoen. (2002) DOUBLE HETEROZYGOSITY FOR Hb PYRGOS [β83(EF7)Gly→Asp] AND Hb E [β26(B8)Glu→Lys] FOUND IN ASSOCIATION WITH α-THALASSEMIA. Hemoglobin 26:2, pages 191-196.
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I. Borg, M. Valentino, A. Fiorini & A. E. Felice. (1997) HB Setif [α94(GI)ASPàTYR] in Malta. Hemoglobin 21:1, pages 91-96.
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L. Manca, B. Masala, M. Manca, P. Ferranti & P. Pucci. (1994) Hb G-Miwlo [α64(E13)ASP→ASN] Observed in a Caucasian Family. Hemoglobin 18:1, pages 53-56.
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Articles from other publishers (8)

Ravindra Kumar, Sweta Mishra, Ram Swaroop Uikey, Anil Gwal, Amol Mun, Praveen K Bharti & Rajasubramaniam Shanmugam. (2021) De novo heterozygous Hb G-Waimanalo (α64(E13)Asp>Asn, CTG>CCG; HBA1:c.193G>A) variant in a sickle cell disease patient of an Indian tribe. Journal of Clinical Pathology 74:5, pages 336-338.
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P. VERMEERSCH, M. PHILIPPE & W. GOOSSENS. (2008) Co-inheritance of haemoglobin A2 and beta-thalassaemia in cis. International Journal of Laboratory Hematology 30:4, pages 334-338.
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S. FUCHAROEN, S. SINGSANAN, K. SANCHAISURIYA & G. FUCHAROEN. (2005) Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients. Clinical and Laboratory Haematology 27:3, pages 184-189.
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Robert Van Kirk, Linda M. Sandhaus & James D. Hoyer. (2005) The Detection and Diagnosis of Hemoglobin A 2 ' by High-Performance Liquid Chromatography . American Journal of Clinical Pathology 123:5, pages 657-661.
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Maria De Angioletti, Giuseppina Lacerra, Carlo Gaudiano, Gabriella Mastrolonardo, Leonilde Pagano, Lucia Mastrullo, Santa Masciandaro & Clementina Carestia. (2002) Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features. Human Mutation 20:5, pages 358-367.
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Arunee Jetsrisuparb, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen, Surapon Wiangnon & Patcharee Komwilaisak. (2002) Triple Heterozygosity of a Hemoglobin Variant: Hemoglobin Pyrgos With Other Hemoglobinopathies. International Journal of Hematology 75:1, pages 35-39.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Gino Schilirò, Elena Mirabile, Rosario Testa, Giovanna Russo-Mancuso & Salvatore P. Dibenedetto. (1997) Presence of hemoglobinopathies in Sicily: A historic perspective. American Journal of Medical Genetics 69:2, pages 200-206.
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