386 related articles for article (PubMed ID: 31190580)
1. Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India.
Dehury S; Meher S; Patel S; Das K; Jana A; Bhattacharya S; Sahoo S; Sarkar B; Mohanty PK
Hemoglobin; 2019 Mar; 43(2):132-136. PubMed ID: 31190580
[TBL] [Abstract][Full Text] [Related]
2. Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, India.
Meher S; Dehury S; Mohanty PK; Patel S; Pattanayak C; Bhattacharya S; Das K; Sarkar B
Hemoglobin; 2016 Aug; 40(4):270-2. PubMed ID: 27254408
[TBL] [Abstract][Full Text] [Related]
3. Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia.
Dash PM; Sahu PK; Patel S; Mashon RS; Kharat KR; Mukherjee MB
Hemoglobin; 2018 Jul; 42(4):236-242. PubMed ID: 30486691
[TBL] [Abstract][Full Text] [Related]
4. Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family.
Godbole KG; Ramachandran A; Karkamkar AS; Dalal AB
Hemoglobin; 2018 Mar; 42(2):141-142. PubMed ID: 29651865
[TBL] [Abstract][Full Text] [Related]
5. Profiling of 35 Cases of Hb S/Hb E (
Dehury S; Mohanty PK; Patel S; Meher S; Das K; Purohit P; Sahoo S; Ratha J
Hemoglobin; 2021 Nov; 45(6):380-386. PubMed ID: 35243949
[TBL] [Abstract][Full Text] [Related]
6. Hb S (
Azarkeivan A; Cohan N; Niazkar HR; Azizi A; Rad F
Hemoglobin; 2020 Mar; 44(2):109-112. PubMed ID: 32370567
[TBL] [Abstract][Full Text] [Related]
7. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
Moassas F; Nweder MS; Murad H
BMC Pediatr; 2019 Feb; 19(1):61. PubMed ID: 30777047
[TBL] [Abstract][Full Text] [Related]
8. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
[TBL] [Abstract][Full Text] [Related]
9. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (
Nuinoon M; Thipthara O; Fucharoen S
Hemoglobin; 2019 Jan; 43(1):52-55. PubMed ID: 31106603
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling.
Vinciguerra M; Passarello C; Leto F; Crivello A; Fustaneo M; Cassarà F; Cannata M; Maggio A; Giambona A
Hemoglobin; 2016 Aug; 40(4):231-5. PubMed ID: 27258795
[TBL] [Abstract][Full Text] [Related]
13. Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
Sajadpour Z; Amini-Farsani Z; Motovali-Bashi M; Yadollahi M; Khosravi-Farsani N
Hemoglobin; 2020 Jan; 44(1):27-30. PubMed ID: 31899996
[TBL] [Abstract][Full Text] [Related]
14. Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
Gupta RB; Tiwary RS; Pande PL; Kutlar F; Oner C; Oner R; Huisman TH
Hemoglobin; 1991; 15(5):441-58. PubMed ID: 1802886
[TBL] [Abstract][Full Text] [Related]
15. Hemoglobinopathies in the Çukurova Region and Neighboring Provinces.
Yuzbasioglu Ariyurek S; Yildiz SM; Yalin AE; Guzelgul F; Aksoy K
Hemoglobin; 2016 Jun; 40(3):168-72. PubMed ID: 26984585
[TBL] [Abstract][Full Text] [Related]
16. Coinheritance of Hb City of Hope (
Zhou JY; Jiang F; Li J; Chen GL; Li DZ
Hemoglobin; 2019 Mar; 43(2):145-147. PubMed ID: 31268351
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine.
Samha L; Sirdah MM; Reading NS; Karmi B; Agarwal AM
Hemoglobin; 2020 Mar; 44(2):128-130. PubMed ID: 32420772
[TBL] [Abstract][Full Text] [Related]
19. Hb Rush (
Mashon RS; Das R; Dhawan R; Kakkar N; Dhar T
Hemoglobin; 2020 Jan; 44(1):64-66. PubMed ID: 32124638
[TBL] [Abstract][Full Text] [Related]
20. Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family.
Panja A; Chowdhury P; Basu A
Hemoglobin; 2016 Sep; 40(5):300-303. PubMed ID: 27690257
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
