Literature DB >> 7078433

Prevalence of familial hyper- and hypolipoproteinemias: the Princeton School District Family Study.

P M Laskarzewski, P Khoury, J A Morrison, K Kelly, M J Mellies, C J Glueck.   

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Year:  1982        PMID： 7078433     DOI： 10.1016/0026-0495(82)90095-6

Source DB:  PubMed          Journal:  Metabolism        ISSN： 0026-0495            Impact factor:   8.694


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  3 in total

1.  Genetic architecture of lipid traits changes over time and differs by race: Princeton Lipid Follow-up Study.

Authors:  Jessica G Woo; John A Morrison; Davis M Stroop; Lisa Aronson Friedman; Lisa J Martin
Journal:  J Lipid Res       Date:  2014-05-25       Impact factor: 5.922

2.  Cost-effective sib-pair designs in the mapping of quantitative-trait loci.

Authors:  H Zhao; H Zhang; J I Rotter
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

3.  Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.

Authors:  S G Young; S T Hubl; R S Smith; S M Snyder; J F Terdiman
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808
  3 in total

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