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Bu Makaleye Atıf Yap
ÖZSOYLU, Ş. (2015). About Chediak-Higashi, Hemoglobin Lansing, and Hemoglobin Jabalpur. Turkish Journal of Hematology, Cilt: 32 - Sayı: 1, 90–91. https://ajindex.com/articles/413119
Dergiler / Turkish Journal of Hematology / 2015 / Cilt: 32 - Sayı: 1
About Chediak-Higashi, Hemoglobin Lansing, and Hemoglobin Jabalpur
- Sayfa
- 90–91
- DOI
- —
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗Kaynakça (4)
- Karabel M, Kelekçi S, Sen V, Karabel D, Aliosmanoglu C, Söker M. A rare cause of recurrent oral lesions: Chediak- Higashi syndrome. Turk J Hematol 2014;31:313-314
- Takahara S, Hamilton HB, Neel JV, Kobara TY, Ogura Y, Nishimura ET. Hypocatalasemia: a new genetic carrier state. J Clin Invest 1960;39:610-619
- Akar N, Torun D, Öztürk A. Hemoglobin Lansing (alpha) [HBA2 CD87 (HIS>GLU) (C>A)] in a Turkish individual resulting from another nucleotide substitution. Turk J Hematol 2014;31:317-318
- Colak A, Toprak B, Yararbas K, Akyol F, Ceylan C. First observation of hemoglobin Jabalpur [beta 3 (NA3) Lac>Pro] in the Turkish population. Turk J Hematol 2014;31:319- 320.