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Hemoglobin
international journal for hemoglobin research
Volume 31, 2007 - Issue 2
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Original

Genotypic Correlation Between Six Common β-Thalassemia Mutations and the XmnI Polymorphism in the Moroccan Population

Imane Agouti Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc
,
Catherine Badens Laboratoire de Génétique Moléculaire, Hôpital d'Enfant de la Timone, Marseille, France
,
Ahmed Abouyoub Centre Régional de Transfusion Sanguine de Rabat, Rabat, Maroc
,
Mohamed Khattab Service d'Hémato-Oncologie Pédiatrique, Hôpital d'Enfant, Rabat, Maroc
,
Fouad Sayah Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc
,
Amina Barakat Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, Maroc
&
Mohcine Bennani Laboratoire de Biologie Appliquée, Faculté des Sciences et Techniques, Tanger, MarocCorrespondence[email protected] [email protected]
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Pages 141-149 | Received 24 Jul 2006, Accepted 09 Oct 2006, Published online: 07 Jul 2009

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Fatima-Zahra Alaoui-Ismaili, Achraf Laghmich, Naima Ghailani-Nourouti, Amina Barakat & Mohcine Bennani-Mechita. (2020) XmnI Polymorphism in Sickle Cell Disease in North Morocco. Hemoglobin 44:3, pages 190-194.
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Amein K. Al-Ali, Ahmed Alsulaiman, Alhusain J. Alzahrani, Obeid T. Obeid, Chitti Babu Vatte, Cyril Cyrus, Awatif N. Alnafie, Rudaynah A. Alali, Mohammed Alfarhan, Brian Mozeleski & Martin H. Steinberg. (2020) Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia. Hemoglobin 44:2, pages 78-81.
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Ahmad Shoujaa, Faten Moasses, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2020) Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study. Hemoglobin 44:1, pages 42-46.
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Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2019) Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report. Hemoglobin 43:4-5, pages 283-285.
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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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Amel Haj Khelil, Sabri Denden, Nadia Leban, Houria Daimi, Ramzi Lakhdhar, Gérard Lefranc, Jemni Ben Chibani & Pascale Perrin. (2010) Hemoglobinopathies in North Africa: A Review. Hemoglobin 34:1, pages 1-23.
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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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Articles from other publishers (8)

Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, Ayad Ghanam, Manal Elidrissi Errahhali, Zaina Sidqi, Meryem Ouarzane, Majida Charif, Mohammed Bellaoui, Redouane Boulouiz & Noufissa Benajiba. (2022) Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco. Molecular Genetics & Genomic Medicine 10:8.
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Lilia Romdhane, Nessrine MezziYosr HamdiGhada El-Kamah, Abdelhamid Barakat & Sonia Abdelhak. (2019) Consanguinity and Inbreeding in Health and Disease in North African Populations. Annual Review of Genomics and Human Genetics 20:1, pages 155-179.
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Fadwa Said & Amina Abdel-Salam. (2015) XmnI polymorphism: Relation to β-thalassemia phenotype and genotype in Egyptian Children. Egyptian Journal of Medical Human Genetics 16:2, pages 123-127.
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Nadir Ali, Muhammad Ayyub, Saleem Ahmed Khan, Suhaib Ahmed, Kazim Abbas, Hamid Saeed Malik & Sunila Tashfeen. (2015) Frequency of Gγ-globin promoter −158 (C>T) XmnI polymorphism in patients with homozygous/compound heterozygous beta thalassaemia. Hematology/Oncology and Stem Cell Therapy 8:1, pages 10-15.
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Saqib H. Ansari, Tahir S. Shamsi, Saima Munzir, Mohammed T. Khan, Sajida Erum, Kousar Perveen, Tasneem Farzana, Mushtaq Ashraf, Tabassum Mehboob & Moinuddin Moinuddin. (2013) Gγ- Xmn I Polymorphism. Journal of Pediatric Hematology/Oncology 35:4, pages e153-e156.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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Azza AG Tantawy, Nevine G. Andrawes, Amany Ismaeil, Solaf A. Kamel & Wessam Emam. (2012) Prevalence of Xmnl Gγ polymorphism in Egyptian patients with β-thalassemia major. Annals of Saudi Medicine 32:5, pages 487-491.
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Soledad Gamarra, Guillermo Garcia-Effron, Carmen Monteserin, Isabel Lopez-Villar, Florinda Gilsanz & Joaquín Martinez-Lopez. (2009) -Thalassaemia Major in a Spanish Patient due to a Compound Heterozygosity for CD39 /−28 . Advances in Hematology 2009, pages 1-3.
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