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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 3
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Original Article

A Mismatched-Primer Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Strategy for Rapid Screening of the Polyadenylation Signal Mutation αT-saudi (AATAAA→AATAAG) in the α2-Globin Gene

N. Jassim Salmaniya Medical Center, Manama, Bahrain; INSERM U 458, Hôpital Robert Debré, 75019, Paris, France
,
S. Al-Arrayed Salmaniya Medical Center, Manama, Bahrain
,
N. Gerard INSERM U 458, Hôpital Robert Debré, 75019, Paris, France
,
H. Al-Mukharraq Salmaniya Medical Center, Manama, Bahrain
,
A. Ai-Ajami Salmaniya Medical Center, Manama, Bahrain
,
R. Ramasawmy INSERM U 458, Hôpital Robert Debré, 75019, Paris, France
&
R. Krishnamoorthy INSERM U 458, Hôpital Robert Debré, 75019, Paris, FranceCorrespondence[email protected]
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Pages 213-220 | Received 08 Jan 1999, Accepted 09 Apr 1999, Published online: 07 Jul 2009

Citations (16)

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Madeeha Kamal, Shaza Abu-Sirriya, Aseel Abu-Dayya, Hebah Al-Khatib, Hadeel Abu-Ramadan, Miranda Petrou, Aliaa Amer, Ramin Badii & Marina Kleanthous. (2015) The Molecular Basis of α-Thalassemia in the Qatari Pediatric Population. Hemoglobin 39:5, pages 350-354.
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Nabeel J. Al Moamen, Fawzia Mahdi, Ebtihal Salman, Thabet Ahmed, Ruqaya Abbas, Shaikha Al Arrayed, Hassan Sanad & Al Alawi Ahmed. (2013) Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain. Hemoglobin 37:4, pages 369-377.
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Hamida Mesbah-Amroun, Fatiha Rouabhi, Rolande Ducrocq & Jacques Elion. (2008) Molecular Basis of α-Thalassemia in Algeria. Hemoglobin 32:3, pages 273-278.
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Aisha Al-Obaidli, Mowafak Hamodat, Zainab Fawzi, Mohamed Abu-Laban, Nathalie Gerard & Rajagopal Krishnamoorthy. (2007) Molecular Basis of Thalassemia in Qatar. Hemoglobin 31:2, pages 121-127.
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Hajer Siala, Faida Ouali, Taieb Messaoud, Rachida Sfar & Slaheddine Fattoum. (2005) First Description in Tunisia of a Point Mutation at Codon 119 (CCT→TCT) in the α1-Globin Gene: Hb Groene Hart in Association with the − α3.7 Deletion. Hemoglobin 29:4, pages 263-268.
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Hajer Siala, Slaheddine Fattoum, Taieb Messaoud, Fadiq Ouali, Nathalie Gerard & Rajagopal Krishnamoorthy. (2004) A Novel α‐Thalassemia Nonsense Mutation in Codon 23 of the α2‐Globin Gene (GAG→TAG) in a Tunisian Family. Hemoglobin 28:3, pages 249-254.
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Gerasimos Dimisianos, Joanne Traeger‐Synodinos, Christina Vrettou, Ioannis Papassotiriou & Emmanuel Kanavakis. (2004) A Rare 33 bp In‐Frame Deletion (α63–74 or α64–74 or α65–75) in the α1‐Globin Gene Causing α+‐Thalassemia: A Second Observation. Hemoglobin 28:2, pages 137-143.
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Amine Zorai, Salem Abbes, Claude Préhu, Souheil Omar, Nathalie Gerard, Raouf Hafsia, Bouaziz Asma, Fethi Guemira & Kousay Dellagi. (2003) Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings. Hemoglobin 27:1, pages 57-61.
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Amine Zorai, Cornelis L. Harteveld, Achech Bakir, Peter Van Delft, Abdelaziz Falfoul, Koussay Dellagi, Salem Abbes & Piero C. Giordano. (2002) MOLECULAR SPECTRUM OF α-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH. Hemoglobin 26:4, pages 353-362.
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M. Akif Çürük, Yurdanur Kilinç, Cüneyt Evrüke, Fatma T. Ozgünen, Kýymet Aksoy & Guneş T. Yüreğir. (2001) PRENATAL DIAGNOSIS OF Hb H DISEASE CAUSED BY A HOMOZYGOSITY FOR THEα2 POLY A (AATAAA→ AATAAG) MUTATION. Hemoglobin 25:2, pages 255-258.
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Articles from other publishers (6)

Eleonora Gambineri, Sara Ciullini Mannurita, David Hagin, Marina Vignoli, Stephanie Anover-Sombke, Stacey DeBoer, Gesmar R. S. Segundo, Eric J. Allenspach, Claudio Favre, Hans D. Ochs & Troy R. Torgerson. (2018) Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome. Frontiers in Immunology 9.
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S. Abuamer, D. K. Shome, A. Jaradat, A. Radhi, J. P. Bapat, K. A. Sharif, J. Al‐Touq, A. Al‐Asheeri & A. Al‐Ajami. (2016) Frequencies and phenotypic consequences of association of α‐ and β‐thalassemia alleles with sickle‐cell disease in Bahrain. International Journal of Laboratory Hematology 39:1, pages 76-83.
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Salam S. Alkindi, Shoaib AlZadjali, Shahina Daar, Eunice Sindhuvi, Yasser Wali, Anil V. Pathare, Suresh Venugopal, Claudine Lapoumeroulie, Alok Srivastava & Rajagopal Krishnamoorthy. (2013) A stepwise α-thalassemia screening strategy in high-prevalence areas. European Journal of Haematology 91:2, pages 164-169.
Crossref
H. Siala, F. Ouali, T. Messaoud, A. Bibi & S. Fattoum. (2008) α-Thalassaemia in Tunisia: some epidemiological and molecular data. Journal of Genetics 87:3, pages 229-234.
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Shahina Daar, David Gravell, Hussein M. Hussein, Anil V. Pathare, Yasser Wali & Rajagopal Krishnamoorthy. (2007) Haematological and clinical features of β-thalassaemia associated with Hb Dhofar. European Journal of Haematology 80:1, pages 67-70.
Crossref
B. E. Clark & S. L. Thein. (2004) Molecular diagnosis of haemoglobin disorders. Clinical and Laboratory Haematology 26:3, pages 159-176.
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