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Results: 7

1.

Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia.

Allayee H, Krass KL, Pajukanta P, Cantor RM, van der Kallen CJ, Mar R, Rotter JI, de Bruin TW, Peltonen L, Lusis AJ.

Circ Res. 2002 May 3;90(8):926-31.

PMID:
11988495
[PubMed - indexed for MEDLINE]
Free Article
2.

Unraveling the complex genetics of familial combined hyperlipidemia.

Suviolahti E, Lilja HE, Pajukanta P.

Ann Med. 2006;38(5):337-51. Review.

PMID:
16938803
[PubMed - indexed for MEDLINE]
3.

Inheritance of plasma apolipoprotein B levels in families of patients undergoing coronary arteriography at an early age.

Coresh J, Beaty TH, Kwiterovich PO Jr.

Genet Epidemiol. 1993;10(3):159-76. Review.

PMID:
8349099
[PubMed - indexed for MEDLINE]
4.

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK.

Dan Med Bull. 2002 Nov;49(4):318-45. Review.

PMID:
12553167
[PubMed - indexed for MEDLINE]
5.

Novel genes for familial combined hyperlipidemia.

Aouizerat BE, Allayee H, Bodnar J, Krass KL, Peltonen L, de Bruin TW, Rotter JI, Lusis AJ.

Curr Opin Lipidol. 1999 Apr;10(2):113-22. Review.

PMID:
10327279
[PubMed - indexed for MEDLINE]
6.

From Ag phenotyping to molecular genetics: apolipoprotein B, serum lipid levels and coronary artery disease in Finland.

Tikkanen MJ, Heliƶ T.

Clin Genet. 1994 Jul;46(1 Spec No):71-6. Review. No abstract available.

PMID:
7988082
[PubMed - indexed for MEDLINE]
7.

Genetics and molecular biology.

Chamberlain JC.

Curr Opin Lipidol. 1996 Dec;7(6):U179-83. Review. No abstract available.

PMID:
9117131
[PubMed - indexed for MEDLINE]
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