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rdf:type |
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lifeskim:mentions |
|
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pubmed:issue |
6
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pubmed:dateCreated |
1994-6-29
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pubmed:abstractText |
Recent advances in molecular genetic (DNA) technology have permitted identification of previously undetectable cystic fibrosis (CF) carriers. Although research has been initiated in the general population, to our knowledge no published studies have looked at the utilization of DNA-based carrier screening in the high-risk CF population (family history of CF).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1072-4710
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
148
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
632-7
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:8193692-Adolescent,
pubmed-meshheading:8193692-Adult,
pubmed-meshheading:8193692-Aged,
pubmed-meshheading:8193692-Canada,
pubmed-meshheading:8193692-Child,
pubmed-meshheading:8193692-Child, Preschool,
pubmed-meshheading:8193692-Cross-Sectional Studies,
pubmed-meshheading:8193692-Cystic Fibrosis,
pubmed-meshheading:8193692-DNA,
pubmed-meshheading:8193692-Female,
pubmed-meshheading:8193692-Genetic Counseling,
pubmed-meshheading:8193692-Genetic Testing,
pubmed-meshheading:8193692-Heterozygote Detection,
pubmed-meshheading:8193692-Humans,
pubmed-meshheading:8193692-Infant,
pubmed-meshheading:8193692-Male,
pubmed-meshheading:8193692-Middle Aged,
pubmed-meshheading:8193692-Mutation,
pubmed-meshheading:8193692-Risk Factors
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pubmed:year |
1994
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pubmed:articleTitle |
Cystic fibrosis carrier screening in a high-risk population. Participation based on a traditional recruitment process.
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pubmed:affiliation |
Division of Genetics, Children's Hospital of Eastern Ontario, Ottawa.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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