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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2002-12-13
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pubmed:abstractText |
Polycystic liver disease (PCLD), a dominantly inherited condition separate from polycystic kidney disease (PKD), has recently been found to be linked to a locus on chromosome 19p13.2-13.1 in two North American families. Our aim was to study whether there is clinical or genetic heterogeneity within PCLD families.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0168-8278
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
39-43
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:12480558-Adult,
pubmed-meshheading:12480558-Chromosome Mapping,
pubmed-meshheading:12480558-Chromosomes, Human, Pair 19,
pubmed-meshheading:12480558-Cysts,
pubmed-meshheading:12480558-Decompression, Surgical,
pubmed-meshheading:12480558-Female,
pubmed-meshheading:12480558-Finland,
pubmed-meshheading:12480558-Genetic Linkage,
pubmed-meshheading:12480558-Genetic Variation,
pubmed-meshheading:12480558-Humans,
pubmed-meshheading:12480558-Liver Diseases,
pubmed-meshheading:12480558-Male,
pubmed-meshheading:12480558-Pedigree,
pubmed-meshheading:12480558-Severity of Illness Index
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pubmed:year |
2003
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pubmed:articleTitle |
Polycystic liver disease is genetically heterogeneous: clinical and linkage studies in eight Finnish families.
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pubmed:affiliation |
Department of Human Molecular Genetics, National Public Health Institute, Mannerheimintie 166, 00300 Helsinki, Finland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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