27 related articles for article (PubMed ID: 32508152)
1. Splice Acceptor Mutation [
Waye JS; Hanna M; Nakamura L; Walker L; Eng B; Nfonsam LE
Hemoglobin; 2024 Mar; 48(2):116-117. PubMed ID: 38360540
[TBL] [Abstract][Full Text] [Related]
2. [Evaluation of hemogram in patients with homozygous sickle cell disease: about 87 cases].
Dahmani F; Benkirane S; Kouzih J; Woumki A; Mamad H; Masrar A
Pan Afr Med J; 2016; 25():240. PubMed ID: 28293356
[TBL] [Abstract][Full Text] [Related]
3. [Epidemiological profile of hemoglobinopathies: a cross-sectional and descriptive index case study].
Dahmani F; Benkirane S; Kouzih J; Woumki A; Mamad H; Masrar A
Pan Afr Med J; 2017; 27():150. PubMed ID: 28904678
[TBL] [Abstract][Full Text] [Related]
4. Haptoglobin gene polymorphism and iron profile in sickle cell disease patients with inflammation in Yaounde, Cameroon.
Tuono RM; Simo JL; Nya PCB; Chedjou JP; Fotsing CBK; Chetcha BC; Tah CF; Tayou CT; Mbatcham WF; Pieme CA
Mol Genet Genomic Med; 2024 Jan; 12(1):e2302. PubMed ID: 37970725
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of sickle cell disease by the technique of PCR.
Singh PJ; Shrivastava AC; Shrikhande AV
Indian J Hematol Blood Transfus; 2015 Jun; 31(2):233-41. PubMed ID: 25825564
[TBL] [Abstract][Full Text] [Related]
6. Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis.
Kirkham JK; Estepp JH; Weiss MJ; Rashkin SR
JAMA Netw Open; 2023 Oct; 6(10):e2337484. PubMed ID: 37851445
[TBL] [Abstract][Full Text] [Related]
7. The
Lakkakula BVKS; Pattnaik S
J Pediatr Genet; 2023 Jun; 12(2):129-134. PubMed ID: 37090825
[TBL] [Abstract][Full Text] [Related]
8. Genetic factors affecting clinical severity in beta-thalassemia syndromes.
Winichagoon P; Fucharoen S; Chen P; Wasi P
J Pediatr Hematol Oncol; 2000; 22(6):573-80. PubMed ID: 11132233
[TBL] [Abstract][Full Text] [Related]
9. Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.
Ashley-Koch A; Yang Q; Olney RS
Am J Epidemiol; 2000 May; 151(9):839-45. PubMed ID: 10791557
[TBL] [Abstract][Full Text] [Related]
10.
Alaoui-Ismaili FZ; Laghmich A; Ghailani-Nourouti N; Barakat A; Bennani-Mechita M
Hemoglobin; 2020 May; 44(3):190-194. PubMed ID: 32508152
[TBL] [Abstract][Full Text] [Related]
11. Genotypic correlation between six common beta-thalassemia mutations and the XmnI polymorphism in the Moroccan population.
Agouti I; Badens C; Abouyoub A; Khattab M; Sayah F; Barakat A; Bennani M
Hemoglobin; 2007; 31(2):141-9. PubMed ID: 17486495
[TBL] [Abstract][Full Text] [Related]
12. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
Charoenkwan P; Teerachaimahit P; Sanguansermsri T
Hemoglobin; 2014; 38(5):335-8. PubMed ID: 25238043
[TBL] [Abstract][Full Text] [Related]
13. Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant.
Bhanushali AA; Himani K; Patra PK; Das BR
Hemoglobin; 2017; 41(4-6):317-320. PubMed ID: 29313433
[TBL] [Abstract][Full Text] [Related]
14. Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
Muszlak M; Pissard S; Badens C; Chamouine A; Maillard O; Thuret I
Hemoglobin; 2015; 39(3):156-61. PubMed ID: 25806420
[TBL] [Abstract][Full Text] [Related]
15. Hb S/
Belisário AR; Carneiro-Proietti AB; Sabino EC; Araújo A; Loureiro P; Máximo C; Flor-Park MV; Rodrigues DDOW; Ozahata MC; McClure C; Mota RA; Gomes Moura IC; Custer B; Kelly S;
Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
[TBL] [Abstract][Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
