Detalhe da pesquisa
1.
Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis.
Fertil Steril
; 83(2): 513-5, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15705409
2.
WT1 deletion leading to severe 46,XY gonadal dysgenesis, Wilms tumor and gonadoblastoma: case report.
Horm Res Paediatr
; 83(3): 211-6, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25613702
3.
Expression analysis of subtractively enriched libraries (EASEL): a widely applicable approach to the identification of differentially expressed genes.
J Biochem Biophys Methods
; 57(1): 17-33, 2003 Jul 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-12834960
4.
A comprehensive gene mutation screen in men with asthenozoospermia.
Fertil Steril
; 95(3): 1020-4.e1-9, 2011 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21255775
5.
Mortality risk of untreated myosin-binding protein C-related hypertrophic cardiomyopathy: insight into the natural history.
J Am Coll Cardiol
; 58(23): 2406-14, 2011 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-22115648
6.
Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding.
Hum Reprod Update
; 10(6): 533-9, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15465836
7.
Absence of mutations in the PCI gene in subfertile men.
Mol Hum Reprod
; 10(11): 807-13, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15377716
8.
Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern.
Hum Reprod
; 19(1): 71-6, 2004 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-14688159
9.
Chromosomal region 11p15 is associated with male factor subfertility.
Mol Hum Reprod
; 9(10): 587-92, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12970396