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Article

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13

1 Jun 1999

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10369249
DOI: 10.1038/9635

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 11 closest

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13PMID 10369249Read ↗

Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping resultsSemantic proximity Read ↗

Modifier genes in cystic fibrosis.Semantic proximity Read ↗

Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.Semantic proximity Read ↗

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.Semantic proximity Read ↗

Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.Semantic proximity Read ↗

Gene modifiers in pediatrics: application to cystic fibrosis.Semantic proximity Read ↗

Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.Semantic proximity Read ↗

A maternally inherited chromosome 18q22.1 deletion in a male with late‐presenting diaphragmatic hernia and microphthalmia–evaluation of <i>DSEL</i> as a candidate gene for the diaphragmatic defectSemantic proximity Read ↗

Identification of a nonframeshift 84-bp deletion in exon 13 of the cystic fibrosis gene.Semantic proximity Read ↗

Cloning, structure and assignment to Chromosome 19q13 of the human Kir2.4 inwardly rectifying potassium channel gene (KCNJ14)Semantic proximity Read ↗

Molecular diagnosis of cystic fibrosis in Maritime Canada.Semantic proximity Read ↗

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