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Ouwel, A.M. van den
( A.M. van den Ouwel)
azoospermia abnormality mutation vas deferens chromosome infertility oligozoospermia patient fibrosis y chromosome deferen hypogonadism deletion factor region cftr gene microdeletion cbavd analysis absence study reprod cftr gene mutation testicular semen analysis 508/- varicocele semen couple risk factors karyotype cytogenetic sperm 150 men failure chromosome abnormalities azfc region accessory gland infection study 150 men chromosomal cryptorchidism genet cftr mutation y chromosome microdeletions y chromosomal microdeletions laboratory exon 9 translocation transmembrane simoni regulator scrotal counselling examination cryptozoospermia result conductance screening dohle 36 men spermatogenic failure chloride excretion infection non-obstructive azoospermia department offspring c regions protein defect marker chromosome reijo history spermatogenic defects testicular failure cytogenetic abnormalities cftr protein 9 men scrotal surgery table marker
1 Most Recent Publications
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Genetic risk factors in infertile men with severe oligozoospermia and azoospermia
(Article)
Dohle, G.R. Halley, D.J.J. Hemel, J.O. van Ouwel, A.M. van den Pieters, M.H. Weber, R.F.A. Govaerts, L.C. |
2002-01-01
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