Cytogenetic and molecular genetic investigations

Andrology: Male Reproductive Health and Dysfunction

Volumn , Issue , 2010, Pages 119-124

  Simoni, Manuela ^a   Wieacker, Peter ^b  

^a UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^b UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 78049411141     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-540-78355-8_8     Document Type: Chapter

References (7)

1. Egozcue S, Blanco JL, Vendrall JM Garcia F, Veiga A, Aran B, Barri PN, Vidal F, Egozcue J (2000) Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update 6:93-105
2. Ferlin A, Arredi B, Speltra E, Cazzadore C, Selice R, Garolla A, Lenzi A, Foresta C (2007) Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy. J Clin Endocrinol Metab 92:762-770
3. Foresta C, Garolla A, Bartoloni L, Bettella A, Ferlin A (2005) Genetic abnormalities among severely oligospermic men who are candidates for intracytoplasmic sperm injection. J Clin Endocrinol Metab 90:152-156
4. Kamischke A, Gromoll J, Simoni M, Behre HM, Nieschlag E (1999) Transmission of a Y chromosomal deletion involving the deleted in azoospermia (DAZ) and chromodomain (CDY1) genes from father to son through intracytoplasmic sperm injection: case report. Hum Reprod 14:2320-2322
5. Simoni M, Nieschlag E (2007) Genetics of hypogonadotropic hypogonadism. Horm Res 67(Suppl 1):149-154
6. Simoni M, Bakker E, Krausz C (2004) EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int J Androl 27:240-249
7. Simoni M, Tüttelmann F, Gromoll J, Nieschlag E (2008) Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience. Reprod Biomed Online 16:289-303