From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Genetic Background of the Sickle Cell Disease Pediatric Population of Dakar, Senegal, and Characterization of a Novel Frameshift ?-Thalassemia Mutation [HBB: c.265_266del; p.Leu89Glufs*2].
Hemoglobin 2017 Jul 1-7.
Gueye Tall Fatou, Martin Cyril, Malick Ndour El Hadji, Déme Ly Indou, Renoux Céline, Chillotti Louis, Veyrenche Nicolas, Connes Philippe, Madieye Gueye Papa, Ndiaye Diallo Rokhaya, Lacan Philippe, Diagne Ibrahima, Amadou Diop Pape, Cissé Aynina, Lopez Sall Philomène, Joly Philip - Genome-wide association study of erythrocyte density in sickle cell disease patients.
Blood cells, molecules & diseases 2017 Jun 65 60-65.
Ilboudo Yann, Bartolucci Pablo, Rivera Alicia, Sedzro Josepha-Clara, Beaudoin Mélissa, Trudel Marie, Alper Seth L, Brugnara Carlo, Galactéros Frédéric, Lettre Guillau - Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon.
British journal of haematology 2017 May .
Geard Amy, Pule Gift D, Chetcha Chemegni Bernard, Ngo Bitoungui Valentina J, Kengne Andre P, Chimusa Emile R, Wonkam Ambroi - Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?
Molecular diagnosis & therapy 2017 May .
de Azevedo Laura Alencastro, Bonazzoni Joyce, Wagner Sandrine Comparsi, Farias Mariela Granero, Bittar Christina M, Daudt Liane, de Castro Simone Marti - SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.
BMC research notes 2017 May 10 (1): 183.
Pule Gift Dineo, Bitoungui Valentina Josiane Ngo, Chemegni Bernard Chetcha, Kengne Andre Pascal, Wonkam Ambroi
.png)
No hay comentarios:
Publicar un comentario