SEARCH

SEARCH BY CITATION

References

  • Bartels I., Starke H., Argyriou L., Sauter SM, Zoll B., Liehr T.. An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. Eur J Med Genet. 2007; 50: 133138.
  • Chantot-Bastaraud S., Ravel C., Berthaut I., McElreavey K., Bouchard P., Mandelbaum J., Siffroi JP. Sperm-FISH analysis in a pericentric chromosome 1inversion, 46,XY, inv(1)(p22q42), associated with infertility. Mol Hum Reprod. 2007; 13: 5559.
  • Coco R., Rahn MI, Estanga PG, Antonioli G., Solari AJ. A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: case report. Hum Reprod. 2004; 19 (12): 27842790.
  • Dallapiccola B., de Filippis V., Notarangelo A., Perla G., Zelante L.. Ring chromosome 21 in healthy persons: different consequences in females and in males. Hum Genet. 1986; 73: 218220.
  • Huret JL, Leonard C., Kanoui V.. Ring chromosome 21 in a phenotypically normal but infertile man. Clin Genet. 1985; 28: 541545.
  • Joly-Helas G., de La Rochebrochard C., Mousset-Siméon N., Moirot H., Tiercin C., Romana SP, Le Caignec C., Clavier B., Macé B., Rives N.. Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report. Hum Reprod. 2007; 22: 12921297.
  • Joseph A., Thomas IM. A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility. J Med Genet. 1982; 19: 375377.
  • Lee IW, Su MT, Hsu CC, Lin YH, Chen PY, Kuo PL. Constitutional complex chromosomal rearrangements in azoospermic men: case report and literature review. Urology. 2006; 68: 1343.e5–8.
  • Martin J.R., Wold A., Taylor HS. Ring chromosome 12 and severe oligospermia: a case report. Fertil Steril. 2008; 90: 443.e1315.
  • McIlree ME, Tulloch WS, Newsam JE. Studies on human meiotic chromosomes from testicular tissue. Lancet I. 1966; 679682.
  • Odorisio T., Rodriguez TA, Evans EP, Clarke AR, Burgoyne PS. The meiotic checkpoint monitoring synapsis eliminates spermatocytes via p53-independent apoptosis. Nat Genet. 1998; 18: 257261.
  • Rodriguez MT, Martin MJ, Abrisqueta JA. A complex balanced rearrangement involving four chromosomes in an azoospermic man. J Med Genet. 1985; 22: 6667.
  • Roeder GS, Bailis JM. The pachytene checkpoint. Trends Genet. 2000; 16: 395403.
  • Salahshourifar I., Gilani MA, Vosough A., Tavakolzadeh T., Tahsili M., Mansori Z.. De novo complex chromosomal rearrangement of 46,XY,t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic male. J Appl Genet. 2007; 48: 9394.
  • Siffroi JP, Benzacken B., Straub B., Le Bourhis C., North MO, Curotti G., Bellec V., Alvarez S., Dadoune JP. Assisted reproductive technology and complex chromosomal rearrangements: the limits of ICSI. Mol Hum Reprod. 1997; 3: 847851.
  • Sills ES, Kim JJ, Witt MA, Palermo GD. Non-obstructive azoospermia and maturation arrest with complex translocation 46,XY t(9;13;14)(p22;q21.2;p13) is consistent with the Luciani-Guo hypothesis of latent aberrant autosomal regions and infertility. Cell Chromosome Res. 2005; 4: 2.
  • Slater HR, Nouri S., Earle E., Lo AW, Hale LG, Choo KH. Neocentromere formation in a stable ring 1p32-p36.1 chromosome. J Med Genet. 1999; 36: 914918.
  • Stahl BC, Patil SR, Syrop CH, Sparks AE, Wald M.. Supernumerary minute ring chromosome 14 in a man with primary infertility and left varicocele. Fertil Steril. 2007; 87: 1213.e1–3.
  • Yoshida A., Miura K., Shirai M.. Cytogenetic survey of 1,007 infertile males. Urol Int. 1997; 58: 166176.