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6. [Disease caused by sickle cell anemia and hemoglobin D-Punjab. 3d case found in Venezuela]. Guevara JM; Arends-Merino A; Arends T Sangre (Barc); 1985; 30(2):185-9. PubMed ID: 4012519 [No Abstract] [Full Text] [Related]
7. Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis. Girisha KM; Vahab SA; Dalal AB; Gopinath PM; Satyamoorthy K Ann Hematol; 2010 Jun; 89(6):625-6. PubMed ID: 19727721 [No Abstract] [Full Text] [Related]
8. Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A). Boucher MO; Chui DH; Woda BA; Newburger PE Hemoglobin; 2016 Jun; 40(3):208-9. PubMed ID: 27117572 [TBL] [Abstract][Full Text] [Related]
9. Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion. Faustino P; Picanço I; Miranda A; Seixas T; Ferrão A; Morais A; Lavinha J; Romão L Hemoglobin; 2002 May; 26(2):185-9. PubMed ID: 12144063 [No Abstract] [Full Text] [Related]
10. [Double heterozygote hemoglobin D/B0 thalassemia. Report of 3 cases in a Portuguese family]. Sousa Uva L; Fernandes A; Pilar M Nouv Rev Fr Hematol (1978); 1983; 25(6):387-90. PubMed ID: 6664837 [TBL] [Abstract][Full Text] [Related]
11. Hemoglobin Savaria--alpha 49(CE7)Ser----Arg in the United States. Suarez CR; Jue DL; Moo-Penn WF Hemoglobin; 1985; 9(6):627-9. PubMed ID: 3937825 [No Abstract] [Full Text] [Related]
12. Hb Capa or alpha (2)94(G1)Asp-->Gly beta 2, a mildly unstable variant with an A-->G (GAC-->GGC) mutation in codon 94 of the alpha 1-globin gene. Dinçol G; Dinçol K; Erdem S; Pobedimskaya DD; Molchanova TP; Ye Z; Webber BB; Wilson JB; Huisman TH Hemoglobin; 1994 Jan; 18(1):57-60. PubMed ID: 8195009 [No Abstract] [Full Text] [Related]
14. Association of Hb G-Chinese [alpha30(B11)Glu --> Gln] with alpha-thalassemia-1 of the Thai type in a Taiwanese family. Shih MC; Peng CT; Chang JG Hemoglobin; 2003 Feb; 27(1):41-4. PubMed ID: 12603093 [No Abstract] [Full Text] [Related]
15. The first case of Hb E-Saskatoon associated with Hb Lepore-Baltimore found in Spain. Ropero P; Murga MJ; González FA; Polo M; Benavente C; Salvador M; Villegas A Hemoglobin; 2005; 29(3):215-9. PubMed ID: 16114185 [TBL] [Abstract][Full Text] [Related]
16. Molecular diagnosis of a case of Hb Phnom Penh [alpha117(GH5)Phe-I1e-alpha118(H1)Thr (alpha1)]. Leung RY; Ma ES; Chan AY; Chow EY Hemoglobin; 2006; 30(3):397-9. PubMed ID: 16840232 [TBL] [Abstract][Full Text] [Related]
17. Double heterozygosity for hemoglobin E and a Lepore-type hemoglobin found in a Thai woman. Boontrakoonpoontawee P; Svasti J; Fucharoen S; Winichagoon P Birth Defects Orig Artic Ser; 1987; 23(5A):269-74. PubMed ID: 3689906 [No Abstract] [Full Text] [Related]
18. Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia. Giordano PC; Harteveld CL; Streng H; Oosterwijk JC; Heister JG; Amons R; Bernini LF Hemoglobin; 1994 Jan; 18(1):11-8. PubMed ID: 8195005 [TBL] [Abstract][Full Text] [Related]
19. [Hemoglobin D Punjab. Apropos of 2 families]. Brügger E; Favre H; Waldvogel F; Boreux G; Miescher PA; Klein D; Wyss M Schweiz Med Wochenschr; 1979 Aug; 109(32):1187-93. PubMed ID: 158829 [TBL] [Abstract][Full Text] [Related]
20. Co-inheritance of hemoglobin D-punjab and hemoglobin S: case report. Athanasiou-Metaxa M; Economou M; Tsatra I; Pratsidou P; Tsantali C J Pediatr Hematol Oncol; 2002; 24(5):421. PubMed ID: 12142798 [No Abstract] [Full Text] [Related] [Next] [New Search]