Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study - Concepedia

Concepedia

Publication | Open Access

Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study

DOI Full Paper Access

34

Citations

16

References

2004

Year

Kristin G. Monaghan, W. Edward Highsmith, J. Amos, Victoria M. Pratt, B. Roa, Michael J. Friez, Lisa Pike-Buchanan, I. Buyse, Joy B. Redman, C. Ström,

Genetics in Medicine

Mendelian DisorderGenetic DisorderMedicineGeneticsClinical GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationPublic HealthMolecular DiagnosticsGenotype-phenotype CorrelationI148t CarriersVariant InterpretationMonogenic DisordersCystic Fibrosis Mutation

References

	Year	Citations

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