SavedAdd your journal

Journals / Turkish Journal of Hematology / 2016 / Cilt: 33 - Sayı: 1

First Observation of Hemoglobin G-Waimanalo and Hemoglobin

Duran CANATAN
TÜRKER BİLGEN
Vildan ÇİFTÇİ
Gülsüm YAZICI
Serpil DELİBAŞ
İBRAHİM KESER
Pages
71–72
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
🔖

Cite This Article

CANATAN, D., BİLGEN, T., ÇİFTÇİ, V., YAZICI, G., DELİBAŞ, S., KESER, İ. (2016). First Observation of Hemoglobin G-Waimanalo and Hemoglobin. Turkish Journal of Hematology, Cilt: 33 - Sayı: 1, 71–72. https://ajindex.com/articles/412477

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Harteveld CL, Higgs DR. Alpha-thalassaemia. Orphanet J Rare Dis 2010;5:13
  2. Blackwell RQ, Jim RT, Tan TG, Weng MI, Liu CS, Wang CL. Hemoglobin G Waimanalo: alpha-64 Asp leads to Asn. Biochim Biophys Acta 1973;322:27-33
  3. Brennan SO, Chan T, Ryken S, Ruskova A. A second case of Hb Fontainebleau [alpha21(B2)Ala-->Pro] in an individual with microcytosis. Hemoglobin 2009;33:258-261
  4. Akar N. An updated review of abnormal hemoglobins in the Turkish population. Turk J Hematol 2014;31:97-98
  5. Lin M, Wu JR, Yang LY, Chen H, Wang PP, Wang Q, Zheng L. Hb G-Waimanalo: occurrence in combination with alpha-thalassemia-1 Southeast Asian deletion. Blood Cells Mol Dis 2009;42:36-37
  6. Tan TG, Jim RT, Blackwell RQ. Hemoglobin G Waimanalo beta thalassemia. Hawaii Med J 1978;37:235-239
  7. Lin M, Wang Q, Zheng L, Huang Y, Lin F, Lin CP, Yang LY. Prevalence and molecular characterization of abnormal hemoglobin in eastern Guangdong of southern China. Clin Genet 2012;81:165-171
  8. Wajcman H, Blouquit Y, Gombaud-Saintonge G, Riou J, Galacteros F.Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin. Hemoglobin 1989;13:421-428
  9. Turner A, Sasse J, Varadi A. Hb Fontainebleau (HBA2: c.64G>C) in the United Arab Emirates. Hemoglobin 2014;38:216-220.