Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling

Samankaltaisia teoksia

• Congenital Bilateral Absence of the Vas Deferens as an Atypical Form of Cystic Fibrosis: Reproductive Implications and Genetic Counseling
  Tekijä: de Souza, Denise Andréa Silva, et al.
  Julkaistu: (2017)
• Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels.
  Tekijä: Mickle, J E, et al.
  Julkaistu: (2000)
• Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens
  Tekijä: Havasi, Viktoria, et al.
  Julkaistu: (2010)
• Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies
  Tekijä: Gajbhiye, Rahul, et al.
  Julkaistu: (2016)
• Medical genetics: advances in brief: Congenital bilateral absence of vas deferens in the absence of cystic fibrosis
  Tekijä: Barnicoat, Angela
  Julkaistu: (1995)