These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
62. A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [β7(A4)Glu→Lys; Guan ZY; Zhong ZY; Xu ZB; Chen JH; Liu YH Hemoglobin; 2022 Nov; 46(6):338-340. PubMed ID: 36691989 [TBL] [Abstract][Full Text] [Related]
63. First Spanish case of thalassemia major due to a compound heterozygosity for the IVS-II-848 (C --> A) and codon 39 (C --> T) mutations of the beta-globin gene. Ropero P; Villegas A; Muñoz J; Briceño O; Mora A; Salvador M; Polo M; González FA Hemoglobin; 2006; 30(1):15-21. PubMed ID: 16540410 [TBL] [Abstract][Full Text] [Related]
65. Molecular characterization of hereditary persistence of fetal hemoglobin in the Karen people of Thailand. Trachoo O; Sura T; Sakuntabhai A; Singhasivanon P; Krudsood S; Phimpraphi W; Krasaesub S; Chanjarunee S; Looareesuwan S Hemoglobin; 2003 May; 27(2):97-104. PubMed ID: 12779271 [TBL] [Abstract][Full Text] [Related]
66. Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients. Camaschella C; Mazza U; Roetto A; Gottardi E; Parziale A; Travi M; Fattore S; Bacchiega D; Fiorelli G; Cappellini MD Am J Hematol; 1995 Feb; 48(2):82-7. PubMed ID: 7847345 [TBL] [Abstract][Full Text] [Related]
67. Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients. Fucharoen S; Fucharoen G; Sanchaisuriya K; Surapot S Acta Haematol; 2002; 108(3):157-61. PubMed ID: 12373089 [TBL] [Abstract][Full Text] [Related]
68. beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0]. Adams JG; Steinberg MH; Newman MV; Morrison WT; Benz EJ; Iyer R Proc Natl Acad Sci U S A; 1981 Jan; 78(1):469-73. PubMed ID: 6165992 [TBL] [Abstract][Full Text] [Related]
69. Double heterozygosity for Hb New York [beta 113 GTG-->GAG; VAL-->GLU] and beta degrees-thalassemia mutations manifests as a thalassemia trait. Lee AC; Ma ES; Chan AY; Szeto SC; Chan LC Pediatr Hematol Oncol; 2008; 25(3):227-31. PubMed ID: 18432506 [TBL] [Abstract][Full Text] [Related]
70. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia. So CC; Chan AY; Tsang ST; Lee AC; Au WY; Ma ES; Chan LC Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202 [TBL] [Abstract][Full Text] [Related]
71. A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia. Alauddin H; Kamarudin K; Loong TY; Azma RZ; Ithnin A; Jalil N; Razak NF; Koh-Xuan-Rong D; Ismail E; C-Khai L; Abdul Latiff Z; Alias H; Othman A Hemoglobin; 2018 Jul; 42(4):247-251. PubMed ID: 30623696 [TBL] [Abstract][Full Text] [Related]
72. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China. Jiang F; Zuo L; Li D; Li J; Tang X; Chen G; Zhou J; Lu H; Liao C BMC Med Genet; 2020 Feb; 21(1):43. PubMed ID: 32111191 [TBL] [Abstract][Full Text] [Related]
73. Clinical, hematological and molecular features in Thais with beta-Malay/beta-thalassemia and beta-Malay/HbE. Laosombat V; Wongchanchailert M; Sattayesevana B; Nopparatana C Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():106-9. PubMed ID: 9640610 [TBL] [Abstract][Full Text] [Related]
75. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family. Fucharoen S; Changtrakun Y; Ratanasiri T; Fucharoen G; Sanchaisuriya K Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166 [TBL] [Abstract][Full Text] [Related]
76. Compound heterozygosity for beta(+)-thalassemia [-31 (A-->G)] and a new variant with low oxygen affinity, Hb Sagami [beta139(H17)Asn-->Thr]. Miyazaki A; Nakanishi T; Kishikawa M; Nakagawa T; Shimizu A; Mawjood AH; Imai K; Aoki Y; Kikuchi M Hemoglobin; 1999 Aug; 23(3):267-71. PubMed ID: 10490140 [No Abstract] [Full Text] [Related]
77. 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]
78. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion. Harteveld CL; Versteegh FG; van Leer EH; Starreveld JS; Kok PJ; van Rooijen-Nijdam I; van Delft P; Zanella-Cleon I; Becchi M; Wajcman H; Giordano PC Hemoglobin; 2007; 31(3):313-23. PubMed ID: 17654068 [TBL] [Abstract][Full Text] [Related]
79. Hb Antalya [codons 3-5 (Leu-Thr-Pro-->Ser-Asp-Ser)]: a new unstable variant leading to chronic microcytic anemia and high Hb A2. Keser I; Kayisli OG; Yesilipek A; Ozes ON; Luleci G Hemoglobin; 2001 Nov; 25(4):369-73. PubMed ID: 11791869 [TBL] [Abstract][Full Text] [Related]
80. 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] [Previous] [Next] [New Search]