Pages that link to "Q38916681"
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The following pages link to Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa (Q38916681):
Displaying 7 items.
- Cystic fibrosis on the African continent. (Q30252014) (← links)
- Rate of improvement of CF life expectancy exceeds that of general population--observational death registration study (Q33818393) (← links)
- Meta-analyses of 4 CFTR variants associated with the risk of the congenital bilateral absence of the vas deferens (Q34103034) (← links)
- CFTR Deletion in Mouse Testis Induces VDAC1 Mediated Inflammatory Pathway Critical for Spermatogenesis (Q36092586) (← links)
- The CFTR M470V, intron 8 poly-T, and 8 TG-repeats detection in Chinese males with congenital bilateral absence of the vas deferens (Q37557318) (← links)
- Seminal vesicle agenesis: An uncommon cause of azoospermia (Q37726890) (← links)
- Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling (Q48157786) (← links)