Differences in clinical condition and genotype at time of diagnosis of cystic fibrosis by newborn screening or by symptoms.
Vernooij-van Langen, A M M
Differences in clinical condition and genotype at time of diagnosis of cystic fibrosis by newborn screening or by symptoms. [electronic resource] - Molecular genetics and metabolism - 100-4 p. digital
Publication Type: Journal Article
1096-7206
10.1016/j.ymgme.2014.07.012 doi
Cystic Fibrosis--diagnosis
Cystic Fibrosis Transmembrane Conductance Regulator--genetics
Gene Frequency
Genotype
Humans
Infant
Infant, Newborn
Mutation
Neonatal Screening--methods
Phenotype
Prevalence
Registries
Differences in clinical condition and genotype at time of diagnosis of cystic fibrosis by newborn screening or by symptoms. [electronic resource] - Molecular genetics and metabolism - 100-4 p. digital
Publication Type: Journal Article
1096-7206
10.1016/j.ymgme.2014.07.012 doi
Cystic Fibrosis--diagnosis
Cystic Fibrosis Transmembrane Conductance Regulator--genetics
Gene Frequency
Genotype
Humans
Infant
Infant, Newborn
Mutation
Neonatal Screening--methods
Phenotype
Prevalence
Registries