No abstract available
MeSH terms
-
Cystic Fibrosis / diagnosis
-
Cystic Fibrosis / genetics*
-
Cystic Fibrosis Transmembrane Conductance Regulator / blood
-
Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
-
Genotype
-
Humans
-
Infant, Newborn
-
Introns
-
Male
-
Mutation
-
Neonatal Screening / methods*
-
Polymorphism, Genetic
Substances
-
CFTR protein, human
-
Cystic Fibrosis Transmembrane Conductance Regulator