Absence of familial defective apolipoprotein B-100... [Hum Genet. 1993] - PubMed

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Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100. [Hum Mutat. 1996]
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100.
Benlian P, de Gennes JL, Dairou F, Hermelin B, Ginon I, Villain E, Lagarde JP, Federspiel MC, Bertrand V, Bernard C, et al. Hum Mutat. 1996; 7(4):340-5.
Angiotensin-converting enzyme DD genotype and cardiovascular disease in heterozygous familial hypercholesterolemia. [Circulation. 1998]
Angiotensin-converting enzyme DD genotype and cardiovascular disease in heterozygous familial hypercholesterolemia.
O'Malley JP, Maslen CL, Illingworth DR. Circulation. 1998 May 12; 97(18):1780-3.
Absence of familial defective apolipoprotein B-100 in Japanese patients with familial hypercholesterolaemia. [Lancet. 1995]
Absence of familial defective apolipoprotein B-100 in Japanese patients with familial hypercholesterolaemia.
Nohara A, Yagi K, Inazu A, Kajinami K, Koizumi J, Mabuchi H. Lancet. 1995 Jun 3; 345(8962):1438.
Review Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia. [J Lipid Res. 1990]
Review Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.
Innerarity TL, Mahley RW, Weisgraber KH, Bersot TP, Krauss RM, Vega GL, Grundy SM, Friedl W, Davignon J, McCarthy BJ. J Lipid Res. 1990 Aug; 31(8):1337-49.
Review R3531C mutation in the apolipoprotein B gene is not sufficient to cause hypercholesterolemia. [Arterioscler Thromb Vasc Biol....]
Review R3531C mutation in the apolipoprotein B gene is not sufficient to cause hypercholesterolemia.
Rabès JP, Varret M, Devillers M, Aegerter P, Villéger L, Krempf M, Junien C, Boileau C. Arterioscler Thromb Vasc Biol. 2000 Oct; 20(10):E76-82.

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Absence of familial defective apolipoprotein B-100 in Israeli patients with domi...
Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction.
Hum Genet. 1993 Apr ;91(3):299-300.

PubMed
Orthorhombic crystal structure of the A-DNA octamer d(GTACGTAC). Comparison with...
Orthorhombic crystal structure of the A-DNA octamer d(GTACGTAC). Comparison with the tetragonal structure.
Eur J Biochem. 1993 Apr 15 ;213(2):673-82.

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Novel expression of human chorionic gonadotropin/luteinizing hormone receptor ge...
Novel expression of human chorionic gonadotropin/luteinizing hormone receptor gene in brain.
Endocrinology. 1993 May ;132(5):2262-70.

PubMed
A pilot controlled study of fluoxetine for obsessive-compulsive symptoms in chil...
A pilot controlled study of fluoxetine for obsessive-compulsive symptoms in children with Tourette's syndrome.
Clin Neuropharmacol. 1993 Apr ;16(2):167-72.

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Multicentre study of l-alpha-glyceryl-phosphorylcholine vs ST200 among patients ...
Multicentre study of l-alpha-glyceryl-phosphorylcholine vs ST200 among patients with probable senile dementia of Alzheimer's type.
Drugs Aging. 1993 Mar-Apr ;3(2):159-64.

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Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction.

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