Pages that link to "Q39253889"
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The following pages link to Comprehensive and rapid genotyping of mutations and haplotypes in congenital bilateral absence of the vas deferens and other cystic fibrosis transmembrane conductance regulator-related disorders (Q39253889):
Displaying 12 items.
- Clinical genetic testing for male factor infertility: current applications and future directions (Q26996604) (← links)
- Clinical evaluation of the infertile male with respect to genetic etiologies (Q33785205) (← links)
- A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo (Q34084248) (← links)
- Evaluation of the azoospermic male (Q34104721) (← links)
- Genetic evaluation of male infertility (Q36450914) (← links)
- WGA allows the molecular characterization of a novel large CFTR rearrangement in a black South African cystic fibrosis patient (Q36944273) (← links)
- Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols (Q37084060) (← links)
- Recommendations for the classification of diseases as CFTR-related disorders (Q37887199) (← links)
- Genetics of male infertility (Q38167117) (← links)
- Pregnancy outcomes after assisted human reproduction (Q38180208) (← links)
- Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers (Q44788767) (← links)
- Genetic diagnosis in practice: From cystic fibrosis to CFTR-related disorders (Q90334333) (← links)