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The relationship between genotype and phenotype in cystic fibrosis.
E. Kerem
*
,
B. Kerem
*
Corresponding author for this work
Research output
:
Contribution to journal
›
Review article
›
peer-review
25
Scopus citations
Overview
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Dive into the research topics of 'The relationship between genotype and phenotype in cystic fibrosis.'. Together they form a unique fingerprint.
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Keyphrases
Cystic Fibrosis Transmembrane Conductance Regulator
100%
Genotype
100%
Cystic Fibrosis
100%
Protein Production
66%
RNA Transcripts
66%
Messenger RNA (mRNA)
66%
Sweat Chloride
33%
Meconium Ileus
33%
Mild mutation
33%
ΔF508
33%
Normal Function
33%
Conductance
33%
High Incidence
33%
In Vitro Study
33%
Exon Skipping
33%
Protein Function
33%
Protein Processing
33%
Pancreatic Insufficiency
33%
RNA-protein Complex
33%
Age at Diagnosis
33%
Uncommon mutation
33%
Lung Disease
33%
Cryptic Exon
33%
Clinical Expression
33%
Severe Phenotype
33%
Mild Phenotype
33%
Class II mutations
33%
Poor nutritional Status
33%
Medicine and Dentistry
Cystic Fibrosis Transmembrane Conductance Regulator
100%
Cystic Fibrosis
100%
In Vitro
33%
Protein Processing
33%
Exon
33%
Exon Skipping
33%
Pancreatic Insufficiency
33%
Cloning
33%
Silo-Filler's Disease
33%
Sweat
33%
Regulator Gene
33%
Meconium ileus
33%
Nutritional Status
33%
Messenger RNA Precursor
33%
Messenger RNA
33%
Biochemistry, Genetics and Molecular Biology
Cystic Fibrosis Transmembrane Conductance Regulator
100%
Cystic Fibrosis
100%
Genotyping
100%
Exon
33%
Posttranslational Modification
33%
Exon Skipping
33%
In Vitro Study
33%
Conductance
33%
Locus Control Region
33%
Precursor mRNA
33%
Messenger RNA
33%