Pages that link to "Q53923559"
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The following pages link to congenital bilateral aplasia of the vas deferens (Q53923559):
Displaying 50 items.
- CFTR (Q14864712) (← links)
- The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic data (Q30560702) (← links)
- Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection (Q33888479) (← links)
- Meta-analyses of 4 CFTR variants associated with the risk of the congenital bilateral absence of the vas deferens (Q34103034) (← links)
- Congenital bilateral absence of vas deferens in the absence of cystic fibrosis (Q34326267) (← links)
- Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype (Q34732168) (← links)
- CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens (Q35642996) (← links)
- Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients (Q35643697) (← links)
- Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols (Q37084060) (← links)
- Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies (Q37186580) (← links)
- CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis (Q37955822) (← links)
- 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) (← links)
- Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study (Q39000632) (← links)
- 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) (← links)
- A T3 allele in the CFTR gene exacerbates exon 9 skipping in vas deferens and epididymal cell lines and is associated with Congenital Bilateral Absence of Vas Deferens (CBAVD). (Q40484515) (← links)
- Birth after intracytoplasmic injection of epididymal sperm from a man with congenital bilateral absence of the vas deferens who had a robertsonian translocation (Q40582031) (← links)
- The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis (Q40755222) (← links)
- Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality. (Q40831102) (← links)
- Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities (Q41467883) (← links)
- Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator (CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens (Q42841512) (← links)
- CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders (Q44929275) (← links)
- Different cystic fibrosis transmembrane conductance regulator mutations in Chinese men with congenital bilateral absence of vas deferens and other acquired obstructive azoospermia. (Q45236846) (← links)
- Medical genetics: advances in brief: Congenital bilateral absence of vas deferens in the absence of cystic fibrosis (Q45762364) (← links)
- Activated caspases in thawed epididymal and testicular spermatozoa of patients with congenital bilateral absence of the vas deferens and intracytoplasmic sperm injection outcome (Q46386759) (← links)
- Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population (Q47956246) (← links)
- Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene (Q47964696) (← links)
- Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling (Q48157786) (← links)
- Congenital bilateral absence of the vas deferens: the impact of spermatogenesis quality on intracytoplasmic sperm injection outcomes in 108 men. (Q50580124) (← links)
- Isolated congenital bilateral absence of vas deferens (CBAVD): a rare anomaly and diagnostic dilemma (Q51016729) (← links)
- Successful pregnancy in a case of azoospermia from congenital bilateral absence of vas deferens (CBAVD) using percutaneous epididymal sperm aspiration (PESA) and intracytoplasmic sperm injection (ICSI). (Q51516575) (← links)
- An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis. (Q52584237) (← links)
- [Association of CFTR gene polymorphism with congenital bilateral absence of vas deferens in ethnic Han Chinese patients]. (Q54457884) (← links)
- GM12895 (Q54846202) (← links)
- GM13242 (Q54846387) (← links)
- GM13276 (Q54846415) (← links)
- Two Novel Missense Mutations (R766M and R792G) in Exon 13 of the CFTR Gene in a Patient with Congenital Bilateral Absence of the Vas deferens (Q58277659) (← links)
- Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens (Q60609513) (← links)
- Analysis by mass spectrometry of 100 cystic fibrosis gene mutations in 92 patients with congenital bilateral absence of the vas deferens (Q61822436) (← links)
- Pulmonary Function and Clinical Observations in Men With Congenital Bilateral Absence of the Vas Deferens (Q61822445) (← links)
- A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens (Q61852018) (← links)
- Unilateral renal agenesis associated with congenital bilateral absence of the vas deferens: phenotypic findings and genetic considerations (Q63359050) (← links)
- SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens (Q64110577) (← links)
- Re: Lu et al.: Different cystic fibrosis transmembrane conductance regulator mutations in Chinese men with congenital bilateral absence of the vas deferens and other acquired obstructive azoospermia (Urology 2013;82:824-828). (Q64923114) (← links)
- Congenital bilateral absence of the vas deferens; four personal cases (author's transl) (Q67403937) (← links)
- Congenital bilateral absence of the vas deferens and cystic fibrosis (Q67881891) (← links)
- Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens (Q70886285) (← links)
- Congenital bilateral absence of the vas deferens and cryptorchidism without cystic fibrosis (Q71050413) (← links)
- Does epididymal length in men with congenital bilateral absence of the vas deferens have a correlation with the fertilization rate of epididymal sperm retrieved by micropuncture technique? (Q71307111) (← links)
- A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patients (Q71585878) (← links)
- Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens (Q71604017) (← links)