[I] Wheeler
R.
, 2007. Wikipedia, ÖzgürAnsiklopedi wikipedia.org/w/index.php?title= Hemoglobine
erişim 8.08.2007.
[2]
Dönba
k L., 2005. İnsan Hemoglobin (Hb) Varvantları, KSÜ. Fen Mühendislik Dergisi, 8(2): 13-22. [3] Huisman T.H.J. 1993. The Structure and Function of Normal and Abnormal Hemoglobins, Bailliere's
ClinicalHaematology, 6: 1-30. [4] Lukens J.N., Lee G.R. 1993. The Abnormal Hemoglobins, IVintrobe's Clinical Hematology, Lea and
Febiger Com., Pennsylvenia, Ed. Lee, G.R., Bithell, C.T., Foerster, J., Athens, J.W., Wkens,
J.N). p. 43.
[5] Huisman T.H.J. 1995. Human Hemoglobin. Blod Disease of Infancy and Childhood, Mosby-Year
Book. Inc., St Louis: Ed. Miller, D.R., Baehner, R.L.7.th ed., p. 85. [6] Tokullugil A., Dirican M., Ulukaya E. (Çev. Eds.) 1997. Biyokimya, Nobel Tıp Kitabevleri, İstanbul,
(Champe, P.C., Harvey, R.A. 1994. Biochemistry.) pp. 100-210 [7] Murray R.K., Granner D.K., Mayes P.A., Radwell V.W. 1988. Harper's Biochemistry. 21.th ed., Long
Medical Book, London. pp. 57-83. [8] Altan N. 2000. Biyokimya. Olgu Sunumlu Yaklaşım, Palme Yayıncılık, Ankara. pp. 1-30. [9] Bunn H.F., Forget B.G. 1986. Hemoglobin: Molecular, Genetic, and Clinical Aspects. W.B. Saunders
Com. Philadelphia .pp. 60-90. [10] Flint, J., Harding, R.M., Boyce, A.J., Cleg, J.B. 1998. The Population Genetics of The
Haemoglobinopathies, Bailliere' s Clinical Haematology, 11: 1-51.
[II]
Başa
k A.N., 2005. Talasemi ve Moleküler genetiği, Moleküler hematoloji ve sitogenetik alt komitesi.
Temel moleküler hematoloji kursu notları. pp. 25-38. [12] Öner C. (Çev. Ed.) 2002. Klug, S., Cummings, M. R. Genetik Kavramlar. Palme Yayıncılık, Ankara.
pp. 55-70
[13] Cavalli-Sforza L., Menozzi P., Piazza A. 1996. The History and Geography of Human Genes,
University Pres, Princeton. p. 276. [14] Flint J., Harding R.M., Boyce A.J., Cleg J.B. 1998. The Population Genetics of The
Haemoglobinopathies. Bailliere' s Clinical Haematology, 11: 1-51. [15] Huisman T.H.J. 1986. The Hemoglobinopathies. Churchill Livingstone Com., Edinburgh. pp. 47-70. [16] Heldlund B. 1980. Hemoglobins of Human Embryos, Fetuses and Neonates. In: Fairbanks VF, ed.
Hemoglobinopaties and talasemias. New York: Brian C Decker, pp. 14-17. [17] Anonim. 2007(a). Anormal hemogloninler sayfasından alınmıştır. www.hemoglobin.
org.tr/bilgi/kitap/hemokitap6.asp erişim: 12/05/2005.
53
HFD SDU Journal of Science {E-Journat), 2011, 6 (1): 40-54
mm
DERGİSİ H)
[18] Huisman T.H.J., Jonxis J.H.P., 1977. The hemoglobinopathies, Techniques of Identification,
NewYork, Marcel Dekker Inc. pp. 24-50. [19] Güngör A.A., Erzurum ve Çevresinde Hemoglobinopatilerin Anormalhemoglobinler ve Talasemi
Mutasyonlarının Moleküler
Tekniklerl
e Belirlenmesi, Doktora tezi, Danışmanı, Prof.Dr. Nazan
Demir, 2008, Erzurum. pp. 69-80.
[20] Basset P., Beuzard Y., Garel M.C., Rosa J. 1978. Isoelectric Focusing of Human Hemoglobin: Its Application to Screening, to The Characterization of 70 Variants, and to The Study of Modified Fractions of Normal Hemoglobins. Blood, 51: 971-982.
[21] Winter W.P., Youdh J. 1983. Interaction of Human Hemoglobin and Its Variants With Agar.
Science, 221: 175-178.
[22] Kutlar F., Kutlar A., Nuguid E., Prchal J., Huismann T.H.J. 1993. Use of HPLC Methodology for the
Chracterization of Combinations of the Common P- Chain Variants HbS, C and O-Arab, and The
a- Chain. Hemoglobin, 17: 55-66. [23] Riou J., Godart C., Hurtrel D., Mathis M., Bimet C., Bardakdjian-Michau J., Prehu C., Wajcman H.,
Galacteros F. 1997. Evaluation of Cation-Exchance High-Performance Liguid-Chromatography
for Presumptive Identification of Hemoglobin Variants. Journal Clinical Chemistry, 43: 34-39. [24] Wajcman H., Bardakdjian J., Ducrocg R. 1993. Structural Charecterization of Abnormal
Hemoglobins from Dried Blood Specimens in a Neonatal Screening Program. Annales de
Biologie Clinique, 50: 867-870. [25] Bain J.B., Ames R.J., Bareford D., Champinon C., Davies S.C., Old J.M., Wild B.J. 1998. The
Laboratuary Diagnosis of Haemoglobinopathies. British Journal of Haematology , 101: 783-792.
[26] Hardison R.C., Chui D.H.K., Giardine B., Riemer C., Patrinos G.P., Anagnou N., Miller W.,
Wajcman H. 2002. Hb Var. A Relational Database of Human Hemoglobin Variants and Thalassemia Mutations at the Globin Gene Server. Human Mutation, 19: 225-233. [27] Zeren F., Genç A., Çürük M.A., 2007. Preliminary data on preimplantion genetic diagnosis for hemoglobinopathies in Turkey, Hemoglobin, 31: 273-277.
[28] Kayrın L., Aksoy K., Tuli A., Çürük MA., Attila G. 2003. Tanıda DNA teknikleri. Adana, 6.
Biyokimya Yaz Okulu. p. 124. [29] Wiggers T. 2005. The Hemoglobınopathıes And Thalassemıas MS, H(ASCP) January, merk
micromedex.com /bmb/bmptables print. Asp? Page.HGBTHAL.DOC erişim: 26.03.2011. [30] Anonim, 2005. European Molecular Genetics Quality Networkweb site
http//www.emqn.org/emqn.php. Prevent_Book_(layout)_v15 erişim: 12/05/2005 [31] Anonim, 2007(c). GATA tıbbi genetik anabilim dalı
http://www.gata.edu.tr/temelbilimler/genetik/akraba_evlilikleri.htm)erişim 28.11.2007
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