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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 3
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Original Article

Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island

Mathias MuszlakService de Pédiatrie, Centre Hospitalier de Mayotte, Mamoudzou, France, Correspondence[email protected]
,
Serge PissardLaboratoire de Génétique, Centre Hospitalier Universitaire Henri Mondor, AP-HP, Paris, France,
,
Catherine BadensDépartement de Génétique Médicale, Centre Hospitalier Universitaire La Timone, AP-HM, Marseille, France,
,
Abdourahim ChamouineService de Pédiatrie, Centre Hospitalier de Mayotte, Mamoudzou, France,
,
Olivier MaillardCellule d’Épidémiologie, Centre Hospitalier de Mayotte, Mamoudzou, France,
&
Isabelle ThuretCentre de Référence des Thalassémies, Service d’Onco-Hématologie Pédiatrique, Centre Hospitalier Universitaire La Timone, AP-HM, Marseille, France
Pages 156-161 | Received 20 Jul 2014, Accepted 15 Oct 2014, Published online: 25 Mar 2015

Citations (8)

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Ahmet Genc, Deniz Tastemir Korkmaz, Suleyman Bayram & Eyyup Rencuzogullari. (2020) The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey. Hemoglobin 44:4, pages 231-239.
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Articles from other publishers (7)

Justin K. Kirkham, Jeremie H. Estepp, Mitch J. Weiss & Sara R. Rashkin. (2023) Genetic Variation and Sickle Cell Disease Severity. JAMA Network Open 6:10, pages e2337484.
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Poonam Tripathi, Sarita Agarwal, Kausik Mandal, Anshul Gupta & Aditya Narayan Sarangi. (2023) Impact of Genetic Polymorphisms in Modifier Genes in Determining Fetal Hemoglobin Levels in Beta-Thalassemia. Thalassemia Reports 13:1, pages 85-112.
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Fatou G. Tall, El hadji M. Ndour, Moustapha Djité, Oumou K. Barry, Pape M. Kandji, Papa M. Gueye, Aynina Cissé & Philoméne Lopez Sall. (2022) Effects of Quantitative Trait Loci (QTLs) of BCL11A and HBS1L-MYB genes on clinical-biological variability of sickle cell disease in a Senegalese pediatric population. African Journal of Biochemistry Research 16:4, pages 71-81.
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L C Rizo-de la Torre, F J Borrayo-López, F J Perea-Díaz, E Aquino, M Venegas, C Hernández-Carbajal, L L Espinoza-Mata & B Ibarra-Cortés. (2022) Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico. Journal of Tropical Pediatrics 68:5.
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Abdourahim Chamouine, Thoueiba Saandi, Mathias Muszlak, Juliette Larmaraud, Laurent Lambrecht, Jean Poisson, Julien Balicchi, Serge Pissard & Narcisse Elenga. (2020) High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte. BMC Pediatrics 20:1.
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Fatou Gueye Tall, Cyril Martin, El Hadji Malick Ndour, Céline Renoux, Indou Déme Ly, Philippe Connes, Papa Madieye Gueye, Rokhaya Ndiaye Diallo, Ibrahima Diagne, Pape Amadou Diop, Aynina Cissé, Philomène Lopez Sall & Philippe Joly. (2019) Combined and differential effects of alpha‐thalassemia and HbF‐quantitative trait loci in Senegalese hydroxyurea‐free children with sickle cell anemia. Pediatric Blood & Cancer.
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Santosh L. Saraf, Titilola S. AkingbolaBinal N. ShahChinedu A. EzekekwuOmowunmi SonubiXu ZhangLewis L. HsuMark T. GladwinRoberto F. Machado, Richard S. Cooper, Victor R. GordeukBamidele O. Tayo. (2017) Associations of α-thalassemia and BCL11A with stroke in Nigerian, United States, and United Kingdom sickle cell anemia cohorts. Blood Advances 1:11, pages 693-698.
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