1. De Kretser DM, Baker HWG. Infertility in men: recent advances and continuing controversies. J Clin Endocrinol Metab 1999; 84(10): 3443-3450.
2. Iammarrone E, Balet R, Lower AM, Gillott C, Grudzinskas JG. Male infertility. Best Pract Res Clin Obstet Gynaecol 2003; 17(2): 211-229.
3. Olesen C, Hansen C, Bendsen E, Byskov AG, Schwinger E, Lopez-Pajares I, Jensen PK, Kristoffersson U, Schubert R, Van Assche E, Wahlstroem J, Lespinasse J, Tommerup N. Identification of human candidate genes for male infertility by digital differential display. Mol Hum Reprod 2001; 7(1): 11-20.
4. Cartwright GE, Edwards CQ, Kravitz K, Skolnick M, Amos DB, Johnson A, Buskjaer L. Hereditary hemo­chromatosis: Phenotypic expression of the disease. N Engl J Med 1979; 301(4): 175-179.
5. Moirand R, Adams PC, Bicheler V, Brissot P, Deugnier Y. Clinical features of genetic hemochromatosis in women compared with men. Ann Intern Med 1997; 127(2): 105-110.
6. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R Jr, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996; 13(4): 399-408.
7. Beutler E, Gelbart T, West C, Lee P, Adams M, Blackstone R, Pockros P, Kosty M, Venditti CP, Phatak PD, Seese NK, Chorney KA, Ten Elshof AE, Gerhard GS, Chorney M. Mutation analysis in hereditary hemochro­matosis. Blood Cells Mol Dis 1996; 22(2): 187-194.
8. Ryan E, O'keane C, Crowe J. Hemochromatosis in Ireland and HFE. Blood Cells Mol Dis 1998; 24(4): 428-432.
9. Campo S, Restuccia T, Villari D, Raffa G, Cuci­notta D, Squadrito G, Pollicino T, Raimondo G. Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin. Liver 2001; 21(4): 233-236.
10. Papanikolaou G, Politou M, Terpos E, Four­lemadis S, Sakellaropoulos N, Loukopoulos D. Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity. Blood Cells Mol Dis 2000; 26(2): 163-168.
11. Fleming RE, Sly WS. Mechanisms of iron accumulation in hereditary hemochromatosis. Annu Rev Phys­iol 2002; 64: 663-680.
12. Hanson EH, Imperatore G, Burke W. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology. Am J Epidemiol 2001; 154(3): 193-206.
13. Mura C, Raguenes O, Ferec C. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis. Blood 1999; 93(8): 2502-2505.
14. Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands. Blood Cells Mol Dis 1999; 25(3-4): 147-155.
15. Wallace DF, Dooley JS, Walker AP. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote. Gastro­enterology 1999; 116(6): 1409-1412.
16. Limdi JK, Crampton JR. Hereditary haemochro­matosis. QJM 2004; 97(6): 315-324.
17. World Health Organization: Laboratory Manual for the Examination of Human Semen and Semen-Cervical Mucus Interaction, 4th ed. Cambridge: Cambridge University Press, 1999.
18. Efremov GD, Dimovski AJ, Plaseska-Karanfilska D, Simjanovska L, Sukarova E, Koceva S. Isolation of genomic DNA from mammalian cells. In: Efremov GD, ed. A Laboratory Manual, 3rd ed. Skopje: Macedonian Academy of Sciences and Arts. 1999:1-3.
19. Beutler E. Genetic irony beyond haemochroma­tosis: clinical effects of HLA-H mutations. Lancet 1997; 349(9048): 296-297.
20. Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP. Haemochro­matosis and HLA-H. Nat Genet 1996; 14(3): 249-251.
21. Beutler E. The significance of the 187G (H63D) mutation in hemochromatosis. Am J Hum Genet 1997; 61(3): 762-764.
22. Fairbanks VF, Brandhagen DJ, Thibodeau SN, Snow K, Wollan PC. H63D is an haemochromatosis associated allele. Gut 1998; 43(3): 441-442.
23. Feder JN, Penny DM, Irrinki A, Lee VK, Lebron JA, Watson N, Tsuchihashi Z, Sigal E, Bjorkman PJ, Schatzman RC. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. Proc Natl Acad Sci USA 1998; 95(4): 1472-1477.
24. Lyon E, Frank E. Hereditary hemochromatosis since the discovery of the HFE gene. Clin Chem 2001; 47(5): 1147-1156.
25. van der Ven K, Fimmers R, Engels G, van der Ven H, Krebs D. Evidence for major histocompatibility complex-mediated effects on spermatogenesis in humans. Hum Reprod 2000; 15(1): 189-196.
26. Miura H, Tsujimura A, Nishimura K, Kitamura M, Kondoh N, Takeyama M, Fujioka H, Sada M, Tsuji T, Matsumiya K, Takahara S, Okuyama A. Susceptibility to idiopathic azoospermia in Japanese men is linked to HLA class I antigen. J Urol 1998; 159(6): 1939-1941.
27. Matsuzaka Y, Makino S, Okamoto K, Oka A, Tsujimura A, Matsumiya K, Takahara S, Okuyama A, Sada M, Gotoh R, Nakatani T, Ota M, Katsuyama Y, Tamiya G, Inoko H. Susceptibility locus for non-obstructive azoospermia is localized within the HLA-DR/DQ subregion: primary role of DQB1*0604. Tissue Antigens 2002; 60(1): 53-63.
28. Maeda T, Nishida J, Nakanishi Y. Expression pattern, subcellular localization and structure – function relationship of rat Tpx-1, a spermatogenic cell adhesion molecule responsible for association with Sertoli cells. Dev Growth Differ 1999; 41(6): 715-722.
29. Branson RE, Grimes SR Jr, Yonuschot G, Irvin JL. The histones of rat testis. Arch Biochem Biophys 1975; 168(2): 403-412.
30. Grimes S, Weisz-Carrington P, Daum H 3rd, Smith J, Green L, Wright K, Stein G, Stein J. A rat his­tone H4 gene closely associated with the testis-specific H1t gene. Exp Cell Res 1987; 173(2): 534-545.
31. Bucci LR, Brock WA, Meistrich ML. Distribution and synthesis of histone 1 subfractions during spermato­genesis in the rat. Exp Cell Res 1982; 140(1): 111-118.
32. Drabent B, Saftig P, Bode C, Doenecke D. Sper­matogenesis proceeds normally in mice without linker histone H1t. Histochem Cell Biol 2000; 113(6): 433-442.
33. Lin Q, Sirotkin A, Skoultchi AI. Normal sper­matogenesis in mice lacking the testis-specific linker his­tone H1t. Mol Cell Biol 2000; 20(6): 2122-2128.
34. Fantz DA, Hatfield WR, Horvath G, Kistler MK, Kistler WS. Mice with a targeted disruption of the H1t gene are fertile and undergo normal changes in structural chromosomal proteins during spermiogenesis. Biol Reprod 2001; 64(2): 425-431.