Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24.

Gemfibrozil in familial combined hyperlipidaemia: effect of added low-dose cholestyramine on plasma and biliary lipids.

Mapping of the familial Mediterranean fever gene to chromosome 16.

Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease.

Lipid and lipoprotein metabolism in familial combined hyperlipidaemia during treatment of sporadic phaeochromocytoma: a case study.

Familial X-linked mental retardation with an X chromosome abnormality.

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.

Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia.

The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1.

The murine situs inversus viscerum (iv) gene responsible for visceral asymmetry is linked tightly to the Igh-C cluster on chromosome 12.

Dysbetalipoproteinaemia: a mixed hyperlipidaemia of remnant lipoproteins due to mutations in apolipoprotein E.

Physical mapping of the human carbonic anhydrase gene cluster on chromosome 8.

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome.

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.

Organization of an Arabidopsis thaliana gene cluster on chromosome 4 including the RPS2 gene, in the Brassica nigra genome.

Factors associated with postprandial lipemia and apolipoprotein A-V levels in individuals with familial combined hyperlipidemia.

N-cadherin gene maps to human chromosome 18 and is not linked to the E-cadherin gene.

B4 Gene Cluster on Chromosome 15 to Tobacco Smoking: From Genetic Association to Mechanism.

Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster.

Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3-Xqter.

Effect of apolipoprotein E polymorphism and XbaI polymorphism of apolipoprotein B on response to lovastatin treatment in familial and non-familial hypercholesterolaemia.

Regulation of the apolipoprotein gene cluster by a long noncoding RNA.

The mouse Col2a-1 gene is highly conserved and is linked to Int-1 on chromosome 15.

The 5-HT2 serotonin receptor gene Htr-2 is tightly linked to Es-10 on mouse chromosome 14.

The genetic architecture of the familial hyperlipidaemia syndromes: rare mutations and common variants in multiple genes.

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Gemfibrozil in familial combined hyperlipidaemia: effect of added low-dose cholestyramine on plasma and biliary lipids.

Mapping of the familial Mediterranean fever gene to chromosome 16.

Relative order and location of DNA sequences on chromosome 21 linked to familial Alzheimer disease.

Lipid and lipoprotein metabolism in familial combined hyperlipidaemia during treatment of sporadic phaeochromocytoma: a case study.

Familial X-linked mental retardation with an X chromosome abnormality.

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.

Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia.

The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1.

The murine situs inversus viscerum (iv) gene responsible for visceral asymmetry is linked tightly to the Igh-C cluster on chromosome 12.

Dysbetalipoproteinaemia: a mixed hyperlipidaemia of remnant lipoproteins due to mutations in apolipoprotein E.

Physical mapping of the human carbonic anhydrase gene cluster on chromosome 8.

Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome.

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.

Organization of an Arabidopsis thaliana gene cluster on chromosome 4 including the RPS2 gene, in the Brassica nigra genome.

Factors associated with postprandial lipemia and apolipoprotein A-V levels in individuals with familial combined hyperlipidemia.

N-cadherin gene maps to human chromosome 18 and is not linked to the E-cadherin gene.

B4 Gene Cluster on Chromosome 15 to Tobacco Smoking: From Genetic Association to Mechanism.

Estimation of Hardy-Weinberg and pairwise disequilibrium in the apolipoprotein AI-CIII-AIV gene cluster.

Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3-Xqter.

Effect of apolipoprotein E polymorphism and XbaI polymorphism of apolipoprotein B on response to lovastatin treatment in familial and non-familial hypercholesterolaemia.

Regulation of the apolipoprotein gene cluster by a long noncoding RNA.

The mouse Col2a-1 gene is highly conserved and is linked to Int-1 on chromosome 15.

The 5-HT2 serotonin receptor gene Htr-2 is tightly linked to Es-10 on mouse chromosome 14.

The genetic architecture of the familial hyperlipidaemia syndromes: rare mutations and common variants in multiple genes.

Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24.

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