Associated Papers
Heterogeneous spectrum of CFTR gene mutations in Chinese patients with CAVD and the dilemma of genetic blocking strategy.
Feng J et al.
Reproduction (cambridge, England), 2022
Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens.
Yang X et al.
Fertility and Sterility, 2015
Function, pharmacological correction and maturation of new Indian CFTR gene mutations.
Sharma H et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society, 2015
Spectrum and distribution of CFTR gene mutations in asthma and chronic pancreatitis cases of North Indian population.
Muthuswamy S et al.
Gene, 2014
Molecular basis of cystic fibrosis disease: an Indian perspective.
Prasad R et al.
Indian Journal of Clinical Biochemistry : Ijcb, 2010
Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.
Sharma N et al.
Human Reproduction (oxford, England), 2009
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