Pages that link to "Q34571667"
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The following pages link to Inactivating mutations of LH and FSH receptors--from genotype to phenotype. (Q34571667):
Displaying 6 items.
- Fetal Leydig cell origin and development (Q33615109) (← links)
- Follicle stimulating hormone receptor gene variants in women with primary and secondary amenorrhea. (Q34038977) (← links)
- Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism. (Q34225321) (← links)
- A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister (Q37323359) (← links)
- Alternative splicing of G protein-coupled receptors: physiology and pathophysiology (Q37560684) (← links)
- 17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence. (Q43628081) (← links)