85 related articles for article (PubMed ID: 19958187)
1. Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families.
Voruganti I; Eng B; Waye JS
Hemoglobin; 2009; 33(6):422-7. PubMed ID: 19958187
[TBL] [Abstract][Full Text] [Related]
2. Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemia.
Lacerra G; Prezioso R; Musollino G; Piluso G; Mastrullo L; De Angioletti M
Eur J Haematol; 2013 Mar; 90(3):214-9. PubMed ID: 23281611
[TBL] [Abstract][Full Text] [Related]
3. Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.
Lou JW; Li Q; Wei XF; Huang JW; Xu XM
Hemoglobin; 2010; 34(4):343-53. PubMed ID: 20642332
[TBL] [Abstract][Full Text] [Related]
4. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
[TBL] [Abstract][Full Text] [Related]
5. A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
Tritipsombut J; Phylipsen M; Viprakasit V; Chalaow N; Sanchaisuriya K; Giordano PC; Fucharoen S; Harteveld CL
Hemoglobin; 2012; 36(6):571-80. PubMed ID: 23181748
[TBL] [Abstract][Full Text] [Related]
6. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
Singha K; Fucharoen G; Hama A; Fucharoen S
Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
[TBL] [Abstract][Full Text] [Related]
7. Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
Patel DK; Patel M; Mashon RS; Patel S; Dash PM; Das BS
Hemoglobin; 2010; 34(6):604-9. PubMed ID: 21077771
[TBL] [Abstract][Full Text] [Related]
8. Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.
Koenig SC; Becirevic E; Hellberg MS; Li MY; So JC; Hankins JS; Ware RE; McMahon L; Steinberg MH; Luo HY; Chui DH
Am J Hematol; 2009 Sep; 84(9):603-6. PubMed ID: 19650141
[TBL] [Abstract][Full Text] [Related]
9. Homozygosity for a rare beta 0-thalassemia mutation [frameshift codons 25/26 (+T)] causes beta-thalassemia intermedia in an Iranian family.
Haghi M; Feizi AA; Harteveld CL; Pouladi N; Feizi MA
Hemoglobin; 2009; 33(1):75-80. PubMed ID: 19205978
[TBL] [Abstract][Full Text] [Related]
10. Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.
Joly P; Lacan P; Garcia C; Couprie N; Francina A
Blood Cells Mol Dis; 2009; 43(1):53-7. PubMed ID: 19269866
[TBL] [Abstract][Full Text] [Related]
11. Mild beta-thalassemia intermedia caused by compound heterozygosity for (G)gamma((A)gammadeltabeta)(o)/beta-thalassemia and molecular characterization of the defect in four Chinese families.
Tan Jin Ai MA; Yap SF; Tan KL; Wong YC; Wee YC; Kok JL
Acta Haematol; 2003; 109(4):169-75. PubMed ID: 12853688
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of a beta-globin gene deletion of 1357 bp in a Taiwanese beta-thalassemia carrier.
Huang CH; Chang YY; Chen CH; Ko TM
Hemoglobin; 2008; 32(5):498-504. PubMed ID: 18932076
[TBL] [Abstract][Full Text] [Related]
13. Identification and molecular characterization of a novel 163 kb deletion: The Italian (ϵγδβ)(0)-thalassemia.
Cardiero G; Prezioso R; Dembech S; Del Vecchio Blanco F; Scarano C; Lacerra G
Hematology; 2016 Jun; 21(5):317-24. PubMed ID: 27077761
[TBL] [Abstract][Full Text] [Related]
14. A Family with γ-Thalassemia and High Hb A2 Levels.
Parmeggiani G; Gualandi F; Selvatici R; Rimessi P; Bigoni S; Taddei Masieri M; Dolcini B; Venturoli A; Cappabianca MP; Ferlini A; Ravani A
Hemoglobin; 2016 Jun; 40(3):187-90. PubMed ID: 27117568
[TBL] [Abstract][Full Text] [Related]
15. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
[TBL] [Abstract][Full Text] [Related]
16. A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous
Zhang X; Yang Y; Zhang H; Du Z; Liu H; Shen Y
Am J Hematol; 2021 Jun; 96(6):E189-E193. PubMed ID: 33651897
[No Abstract] [Full Text] [Related]
17. Application of multiplex ligation-dependent probe amplification to screen for β-globin cluster deletions: detection of two novel deletions in a multi ethnic population.
Cui J; Azimi M; Baysdorfer C; Vichinsky EP; Hoppe CC
Hemoglobin; 2013; 37(3):241-56. PubMed ID: 23577918
[TBL] [Abstract][Full Text] [Related]
18. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes].
Chen JF; Long GF; Lin WX; Chen P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181
[TBL] [Abstract][Full Text] [Related]
19. Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
Wilcox I; Boettger K; Greene L; Malek A; Davis L; Steinberg MH; Luo HY; Chui DH
Am J Hematol; 2009 Jan; 84(1):55-8. PubMed ID: 19006227
[TBL] [Abstract][Full Text] [Related]
20. Molecular identification of the novel Gγ-β hybrid hemoglobin: Hb Gγ-β Ulsan (Gγ through 13; β from 19).
Kim SY; Lee SH; Cho SI; Song SH; Hattori Y; Park SK; Song J; Choi Y; Yang M; Park H; Kim SR; Seong MW; Kim JY; Cho HI; Park SS
Blood Cells Mol Dis; 2010 Dec; 45(4):276-9. PubMed ID: 21035360
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
