323 related articles for article (PubMed ID: 32091272)
21. Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey.
Mendilcioglu I; Yakut S; Keser I; Simsek M; Yesilipek A; Bagci G; Luleci G
Hemoglobin; 2011; 35(1):47-55. PubMed ID: 21250881
[TBL] [Abstract][Full Text] [Related]
22. Prevalence and molecular analysis of β-thalassemia in Adiyaman, Turkey.
Genc A; Tastemir Korkmaz D; Buyukleyla M; Celiker M
Hemoglobin; 2012; 36(2):131-8. PubMed ID: 22356097
[TBL] [Abstract][Full Text] [Related]
23. Premarital screening for thalassemia and sickle cell disease in Saudi Arabia.
Alhamdan NA; Almazrou YY; Alswaidi FM; Choudhry AJ
Genet Med; 2007 Jun; 9(6):372-7. PubMed ID: 17575503
[TBL] [Abstract][Full Text] [Related]
24. Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.
Cürük MA; Zeren F; Genç A; Ozavci-Aygün S; Kilinç Y; Aksoy K
Hemoglobin; 2008; 32(6):525-30. PubMed ID: 19065329
[TBL] [Abstract][Full Text] [Related]
25. Awareness and Attitude of University Students About Screening and Testing for Hemoglobinopathies: Case Study of the Aseer Region, Saudi Arabia.
Eissa M; Patel AA; Farag S; Babiker NH; Al-Shahrani MS; Al-Nahari AM; Al Sahmaa AM; Al-Shraim M
Hemoglobin; 2018 Jul; 42(4):264-268. PubMed ID: 30821195
[TBL] [Abstract][Full Text] [Related]
26. Prevalence of hemoglobinopathies in the Brazilian adult population: National Health Survey 2014-2015.
Rosenfeld LG; Bacal NS; Cuder MAM; Silva AGD; Machado ÍE; Pereira CA; Souza MFM; Malta DC
Rev Bras Epidemiol; 2019; 22Suppl 02(Suppl 02):E190007.SUPL.2. PubMed ID: 31596378
[TBL] [Abstract][Full Text] [Related]
27. Premarital screening of beta-thalassemia trait in the province of Denizli, Turkey.
Keskin A; Türk T; Polat A; Koyuncu H; Saracoglu B
Acta Haematol; 2000; 104(1):31-3. PubMed ID: 11111119
[TBL] [Abstract][Full Text] [Related]
28. Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β
Abdaoui W; Benouareth DE; Djenouni A; Renoux C; Grifi F; Gouri A; Athamnia F; Benalioua M; Joly P
Hemoglobin; 2019; 43(4-5):223-228. PubMed ID: 31603010
[TBL] [Abstract][Full Text] [Related]
29. β-Thalassemia mutations in Western India: outcome of prenatal diagnosis in a hemoglobinopathies project.
Patel AP; Patel RB; Patel SA; Vaniawala SN; Patel DS; Shrivastava NS; Sharma NP; Zala JV; Parmar PH; Naik MR
Hemoglobin; 2014; 38(5):329-34. PubMed ID: 25222044
[TBL] [Abstract][Full Text] [Related]
30. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
Jha AN; Mishra H; Verma HK; Pandey I; Lakkakula BVKS
Hemoglobin; 2018 Mar; 42(2):84-90. PubMed ID: 30200838
[TBL] [Abstract][Full Text] [Related]
31. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
Murad H; Moassas F; Jarjour R; Mukhalalaty Y; Al-Achkar W
Hemoglobin; 2014; 38(6):390-3. PubMed ID: 25405916
[TBL] [Abstract][Full Text] [Related]
32. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
Edison ES; Sathya M; Rajkumar SV; Nair SC; Srivastava A; Shaji RV
Int J Lab Hematol; 2012 Oct; 34(5):556-8. PubMed ID: 22471768
[TBL] [Abstract][Full Text] [Related]
33. Prevalence and spectrum of haemoglobinopathies in females of reproductive age group- A first tertiary care center experience in Punjab, North India.
Narang V; Jain A; Grover S; Soni A; Narang M; Taneja A
Indian J Pathol Microbiol; 2023; 66(3):564-567. PubMed ID: 37530340
[TBL] [Abstract][Full Text] [Related]
34. [Screening for hemoglobinopathies at a knowledge center in Copenhagen. Resources should be allocated to solve a growing health problem in the Nordic countries].
Birgens H
Lakartidningen; 2000 May; 97(22):2752-4. PubMed ID: 10900897
[TBL] [Abstract][Full Text] [Related]
35. Sickle beta 0 thalassemia in Eastern Saudi Arabia.
Pembrey ME; Perrine RP; Wood WG; Weatherall DJ
Am J Hum Genet; 1980 Jan; 32(1):26-41. PubMed ID: 6153864
[TBL] [Abstract][Full Text] [Related]
36. Prevalence of β-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast Turkey.
Incebiyik A; Genc A; Hilali NG; Camuzcuoglu A; Camuzcuoglu H; Kilic A; Vural M
Hemoglobin; 2014; 38(6):402-4. PubMed ID: 25405917
[TBL] [Abstract][Full Text] [Related]
37. Genetic Blood Disorders Survey in the Sultanate of Oman.
Al-Riyami A; Ebrahim GJ
J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
[TBL] [Abstract][Full Text] [Related]
38. Molecular characterization of beta-thalassemia mutations in Guadeloupe.
Romana M; Keclard L; Guillemin G; Lavocat E; Saint-Martin C; Berchel C; Mérault G
Am J Hematol; 1996 Dec; 53(4):228-33. PubMed ID: 8948659
[TBL] [Abstract][Full Text] [Related]
39. Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia.
Al-Ali AK; Alsulaiman A; Alzahrani AJ; Obeid OT; Vatte CB; Cyrus C; Alnafie AN; Alali RA; Alfarhan M; Mozeleski B; Steinberg MH
Hemoglobin; 2020 Mar; 44(2):78-81. PubMed ID: 32448003
[TBL] [Abstract][Full Text] [Related]
40. A comprehensive review of the prevalence of beta globin gene variations and the co-inheritance of related gene variants in Saudi Arabians with beta-thalassemia.
Alaithan MA; AbdulAzeez S; Borgio JF
Saudi Med J; 2018 Apr; 39(4):329-335. PubMed ID: 29619482
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
