3Tuerlings JH,van Golde R J,Oudakker AR,et al.Familial oligoasthenoteratozoospermia:evidence of autosomal dominant inheritance with sex-limited expression[J].Fertil Steril,2002,77(2):415-418.
4Foresta C,Ferlin A,Moro E,et al.Microdeletion of chromosome Y in male infertility:role of the DAZ gene[J].Ann Ital Med Int,2001,16 (2):82-92.
5Slezak R,Sasiadek M.Chromosome Y microdeletions in the pathogenesis of male infertility[J].Pol Merkuriusz Lek,2002,13(75):229-233.
二级参考文献25
1王陪林主编.遗传病学[M].北京:人民卫生出版社,2000.788.
2Madgar I, Dor J, Weissenberg R, et al. Prognostic value of the clinical and laboratory evaluation in patients with nonmosaic Klinefelter syndrome who are receiving assisted reproductive therapy [J]. Fertil Steril, 2002, 77(6) :1167-1169.
4Simon M, Bakker E, Eurlings MCM, et al. Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions [J]. Int J Androl, 1999, 22(5) :292-299.
5Dohle GR, Halley DJ, Van Hemel JO, et al. Genetic risk factor in infertility men with severe oligozoospermia and azoospermia [J].Hum Reprod, 2002, 17(1) :13-16.
6Schulze A, Downward J. Analysis of gene expression by microarrays:cell biologist's gold mine or minefield[J] ? J Cell Sci, 2000,113(23) :4151-4156.
7Phillipson GT, Petrucco OM, Matthews CD. Congenital bilateral absence of the vas deferens cystic fibrosis mutation analysis and intracytoplasmic sperm injection [ J ]. Hum Reprod, 2000, 15(2) :431-435.
8Toth A, Tardy EP, Gombos S, et al. AZFc deletion detected in a newborn with prenatally diagnosis Tq deletion [ J ]. Prenat Giagn, 2001,21(4) :253-255.
9Tachdjian G, Frydman N, Morichon-Delvallez N, et al. Reproductive genetic counseling in non-mosaic 47, XXY patients: implication for preimplantation or prenatal diagnosis:case report and review[J]. Hum Reprod, 2003, 18(2) :271-275.
10Vollrath D, Foote S, Hilton A, et al. The human Y chromosome: a 43-interal map based on naturally occurring deletion [ J ]. Science. 1992. 258(5079) :52-59.
