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Cytogenetic abnormalities and azoospermia factor (AZF) microdeletions in infertile men from Kuwait

By Moussa Alkhalaf and Kamal Al-Shoumer
Topics: Research Letter
Publisher: Library Publishing Media
OAI identifier: oai:pubmedcentral.nih.gov:2893362
Provided by: PubMed Central

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Citations

  1. (2002). A cytogenetic study of Kuwaiti couples with infertility and reproductive disorders: short arm deletion of chromosome 21 is associated with male infertility.
  2. (2005). Azoospermia factor (AZF) in Yq11: towards a molecular understanding of its function for human male fertility and spermatogenesis.
  3. (2001). Chromosomal variants among 1790 infertile men.
  4. (2006). Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders.
  5. (2004). EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art
  6. (2006). Genetic causes of male infertility.
  7. (2009). Genetics of human male infertility.
  8. (1996). Human Y chromosome azoospermia factors (AZF) mapped to different subregions in
  9. (1999). Infertility in Kuwait.
  10. (2007). Primary male infertility in Kuwait: a cytogenetic and molecular study of 289 infertile Kuwaiti patients.
  11. (2008). Underlying karyotype abnormalities in IVF/ICSI patients.
  12. (2006). Y chromosome and male infertility: update.