Associated Papers
Phenotype, genotype and gender identity in a large cohort of patients from India with 5α-reductase 2 deficiency.
Shabir I et al.
Andrology, 2015
[Hereditary prostate cancer].
Heise M et al.
Postepy Higieny I Medycyny Doswiadczalnej (online), 2014
Association of V89L SRD5A2 polymorphism with craving and serum leptin levels in male alcohol addicts.
Lenz B et al.
Psychopharmacology, 2012
Isolated micropenis reveals partial androgen insensitivity syndrome confirmed by molecular analysis.
Bhangoo A et al.
Asian Journal of Andrology, 2010
Small effect of the androgen receptor gene GGN repeat polymorphism on serum testosterone levels in healthy men.
Bogaert V et al.
European Journal of Endocrinology, 2009
[Genetic determinants of anatomical variants of the prostate].
Hamadeh H et al.
Progres En Urologie : Journal De L'association Francaise D'urologie Et De La Societe Francaise D'urologie, 2008
Genetic impact on prostate anatomical variability during ageing: role of CYP17, SRD5A2 and androgen receptor genes polymorphisms.
Larré S et al.
Bju International, 2007
[Molecular basis of hereditary hemochromatosis].
Romanowski T et al.
Postepy Higieny I Medycyny Doswiadczalnej (online), 2006
The 5alpha-reductase type II A49T and V89L high-activity allelic variants are more common in men with prostate cancer compared with the general population.
Giwercman YL et al.
European Urology, 2005
Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.
Simoni M et al.
Human Reproduction Update, 0
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