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7. Hb E and Hb E-like variants in individuals from Turkey. Prozorova-Zamani V; Ozsoylu S; Aksoy M; Headlee MG; Lam H; Wilson JB; Altay C; Huisman TH Hemoglobin; 1981; 5(7-8):743-8. PubMed ID: 7338477 [No Abstract] [Full Text] [Related]
8. Hb Hope [beta 136(H14) Gly----Asp] and Hb E [beta 26(B8)Glu----Lys]: compound heterozygosity in a Thai Mien family. Pillers DA; Jones M; Head C; Jones RT Hemoglobin; 1992; 16(1-2):81-4. PubMed ID: 1634366 [No Abstract] [Full Text] [Related]
9. Hemoglobin E in Indochinese refugees. Cunningham TM West J Med; 1982 Sep; 137(3):186-90. PubMed ID: 7147932 [TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of the fetus at risk for beta-thalassemia/hemoglobin E disease: a report of the first case in Thailand. Kanokpongsakdi S; Winichagoon P; Fucharoen S; Manassagorn J; Tanphaichitr V J Med Assoc Thai; 1987 Jan; 70(1):38-43. PubMed ID: 3572289 [No Abstract] [Full Text] [Related]
12. HPLC-ESI-MS/MS analysis of hemoglobin peptides in tryptic digests of dried-blood spot extracts detects HbS, HbC, HbD, HbE, HbO-Arab, and HbG-Philadelphia mutations. Haynes CA; Guerra SL; Fontana JC; DeJesús VR Clin Chim Acta; 2013 Sep; 424():191-200. PubMed ID: 23796846 [TBL] [Abstract][Full Text] [Related]
13. Hemoglobin Westmead alpha 2 122(H5)His replaced by Gln beta 2: a new hemoglobin variant with the substitution in the alpha 1 beta 1 contact area. Fleming PJ; Hughes WG; Farmilo RK; Wyatt K; Cooper WN Hemoglobin; 1980; 4(1):39-52. PubMed ID: 6153381 [No Abstract] [Full Text] [Related]
14. Interaction of hemoglobin E with other abnormal hemoglobins. Edison ES; Shaji RV; Chandy M; Srivastava A Acta Haematol; 2011; 126(4):246-8. PubMed ID: 21986214 [No Abstract] [Full Text] [Related]
15. Hemoglobin Hotel-Dieu beta 99 Asp replaced by Gly (g1). A new abnormal hemoglobin with high oxygen affinity. Blouquit Y; Braconnier F; Galacteros F; Arous N; Soria J; Zittoun R; Rosa J Hemoglobin; 1981; 5(1):19-31. PubMed ID: 7204092 [TBL] [Abstract][Full Text] [Related]
16. Hemoglobin Rouen (alpha-140 (HC2) Tyr-->His): alteration of the alpha-chain C-terminal region and moderate increase in oxygen affinity. Wajcman H; Kister J; Marden M; Lahary A; Monconduit M; Galacteros F Biochim Biophys Acta; 1992 Oct; 1180(1):53-7. PubMed ID: 1390944 [TBL] [Abstract][Full Text] [Related]
17. Hb Westmead [alpha 122(H5)His----Gln], Hb E [beta 26(B8)Glu----Lys], and alpha-thalassemia-2 (3.7 Kb deletion) in a Laotian family. Gu YC; Gu LH; Wilson JB; Cepreganova B; Ramachandran M; Walker EL; Huisman TH; Potitong P Hemoglobin; 1991; 15(4):297-302. PubMed ID: 1787098 [No Abstract] [Full Text] [Related]
19. Hemoglobin E in a refugee family. Owens MR; Andolina JR; Stein BL N Y State J Med; 1981 Jun; 81(7):1105-7. PubMed ID: 6942257 [No Abstract] [Full Text] [Related]
20. [Identification and characterization of a new hemoglobin variant: hemoglobin Sendagi (beta 42 Phe----Val)]. Ogata K Nihon Ika Daigaku Zasshi; 1987 Feb; 54(1):17-26. PubMed ID: 3593478 [No Abstract] [Full Text] [Related] [Next] [New Search]