Published in J Androl on June 23, 1994
Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials. Am J Respir Crit Care Med (2006) 1.44
Evaluation of the azoospermic male. Asian J Androl (2011) 1.04
Comparative biology of cystic fibrosis animal models. Methods Mol Biol (2011) 1.01
A comprehensive review of genetics and genetic testing in azoospermia. Clinics (Sao Paulo) (2013) 0.96
Recent advances in the genetics of testicular failure. Asian J Androl (2016) 0.94
Predictive factors for sperm retrieval and sperm injection outcomes in obstructive azoospermia: do etiology, retrieval techniques and gamete source play a role? Clinics (Sao Paulo) (2013) 0.89
CFTR interacts with ZO-1 to regulate tight junction assembly and epithelial differentiation through the ZONAB pathway. J Cell Sci (2014) 0.84
Regulation of epithelial function, differentiation, and remodeling in the epididymis. Asian J Androl (2015) 0.76
Meta-analyses of 4 CFTR variants associated with the risk of the congenital bilateral absence of the vas deferens. J Clin Bioinforma (2014) 0.75
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature (1992) 2.63
Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis. JAMA (1992) 2.11
Three additional DNA polymorphisms in the met gene and D7S8 locus: use in prenatal diagnosis of cystic fibrosis. J Pediatr (1987) 1.63
Standardization of PCR amplification for fragile X trinucleotide repeat measurements. Clin Genet (2002) 1.15
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity. Am J Hum Genet (1991) 1.06
Congenital unilateral absence of the vas deferens: a heterogeneous disorder with two distinct subpopulations based upon aetiology and mutational status of the cystic fibrosis gene. Hum Reprod (1995) 0.88
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21. Am J Hum Genet (1988) 0.87
46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies. Am J Med Genet (1993) 0.86
Congenital bilateral absence of the vas deferens and cystic fibrosis. A genetic commonality. World J Urol (1993) 0.83
Relative argininosuccinate synthetase mRNA levels and gene copy number in canavanine-resistant lymphoblasts. Biochim Biophys Acta (1984) 0.82
Pulmonary function and clinical observations in men with congenital bilateral absence of the vas deferens. Chest (1996) 0.82
Dystrophin analysis in duchenne muscular dystrophy: use in fetal diagnosis and in genetic counseling. Am J Hum Genet (1989) 0.79
Prenatal diagnosis and linkage disequilibrium with cystic fibrosis for markers surrounding D7S8. Hum Genet (1990) 0.75
Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probes. Am J Obstet Gynecol (1991) 0.75