No abstract available
MeSH terms
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Alleles*
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Artifacts*
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Cystic Fibrosis / diagnosis*
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Cystic Fibrosis / genetics
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Cystic Fibrosis / prevention & control
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Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
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DNA / genetics*
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DNA / isolation & purification
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DNA Mutational Analysis / methods*
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Feasibility Studies
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Heterozygote
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Homozygote
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Humans
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Leukocytes / chemistry*
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Polymerase Chain Reaction / methods*
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Prenatal Diagnosis / methods*
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Sequence Deletion*
Substances
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CFTR protein, human
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Cystic Fibrosis Transmembrane Conductance Regulator
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DNA