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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

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