Different cystic fibrosis transmembrane conductance regulator mutations in Chinese men with congenital bilateral absence of vas deferens and other acquired obstructive azoospermia.
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[1] R. Prasad,et al. Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens. , 2009, Human reproduction.
[2] Y. Ogawa,et al. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens , 2008, International journal of urology : official journal of the Japanese Urological Association.
[3] Daniel Y. T. Goh,et al. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: a pilot study. , 2006, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[4] Lee-Jun C Wong,et al. Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens. , 2005, Human reproduction.
[5] F. Zacchello,et al. Gender-sensitive association of CFTR gene mutations and 5T allele emerging from a large survey on infertility. , 2005, Molecular human reproduction.
[6] J. Szamatowicz,et al. Cystic fibrosis as a cause of infertility. , 2004, Reproductive biology.
[7] H. Okada,et al. CFTR gene mutations in Japanese individuals with congenital bilateral absence of the vas deferens. , 2003, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[8] R. Sokol. Infertility in men with cystic fibrosis. , 2001, Current opinion in pulmonary medicine.
[9] H. Mei,et al. [Study of CFTR gene mutation in Chinese CUAVD patients]. , 2000, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.
[10] J. Zieleński. Genotype and Phenotype in Cystic Fibrosis , 2000, Respiration.
[11] E. Schwinger,et al. Genetics of male subfertility: consequences for the clinical work-up. , 1999, Human reproduction.
[12] L. Tsui,et al. Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia. , 1999, JAMA.
[13] M. Chernick,et al. Molecular basis of cystic fibrosis in the Republic of Macedonia , 1998, Clinical genetics.
[14] L. Tsui,et al. Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia , 1995, The Lancet.
[15] M Claustres,et al. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. , 1995, The New England journal of medicine.
[16] B. Kerem,et al. Correlation between genotype and phenotype in patients with cystic fibrosis. , 1994, The New England journal of medicine.
[17] F. Collins,et al. Cystic fibrosis: molecular biology and therapeutic implications. , 1992, Science.
[18] S. Kropf,et al. Increased frequency of cystic fibrosis transmembrane conductance regulator gene mutations in infertile males. , 2006, Fertility and sterility.
[19] C. Boeck. Correlation between genotype and phenotype in patients with cystic fibrosis , 1993 .