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1.
OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity.
J Clin Invest
; 133(23)2023 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37847567
2.
Insights on the phenotypic heterogenity of 11ß-hydroxylase deficiency: clinical and genetic studies in two novel families.
Endocrine
; 62(2): 326-332, 2018 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30242600
3.
Trp28Arg/Ile35Thr LHB gene variants are associated with elevated testosterone levels in women with polycystic ovary syndrome.
Gene
; 550(1): 68-73, 2014 Oct 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-25111116
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