Double Msp I RFLP in the human LDL receptor gene

Geisel J, Weisshaar B, Oette K, Mechtel M, Doerfler W (1987)
Nucleic Acids Research 15(9).

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Geisel J, Weisshaar B, Oette K, Mechtel M, Doerfler W. Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research. 1987;15(9).
Geisel, J., Weisshaar, B., Oette, K., Mechtel, M., & Doerfler, W. (1987). Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research, 15(9).
Geisel, J., Weisshaar, B., Oette, K., Mechtel, M., and Doerfler, W. (1987). Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research 15.
Geisel, J., et al., 1987. Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research, 15(9).
J. Geisel, et al., “Double Msp I RFLP in the human LDL receptor gene”, Nucleic Acids Research, vol. 15, 1987.
Geisel, J., Weisshaar, B., Oette, K., Mechtel, M., Doerfler, W.: Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research. 15, (1987).
Geisel, J, Weisshaar, Bernd, Oette, K, Mechtel, M, and Doerfler, W. “Double Msp I RFLP in the human LDL receptor gene”. Nucleic Acids Research 15.9 (1987).
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12 Citations in Europe PMC

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A rare polymorphism in the low density lipoprotein (LDL) gene that affects mRNA splicing.
Bourbon M, Sun XM, Soutar AK., Atherosclerosis 195(1), 2007
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Three novel small deletion mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia.
Chae JJ, Kim SH, Kim UK, Han KH, Kim HS, Kastner DL, Namkoong Y, Park YB, Lee CC., Clin. Genet. 55(5), 1999
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Mutation analysis of exon 3 of the LDL receptor gene in patients with severe hypercholesterolemia.
Geisel J, Gielen J, Oette K, Herrmann W, Wielckens K., Clin. Chem. Lab. Med. 36(5), 1998
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The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark.
Jensen HK, Jensen LG, Hansen PS, Faergeman O, Gregersen N., Atherosclerosis 120(1-2), 1996
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Severe hypercholesterolaemia: unusual inheritance in an Italian pedigree.
Zuliani G, Vigna GB, Corsini A, Maioli M, Romagnoni F, Fellin R., Eur. J. Clin. Invest. 25(5), 1995
PMID: 7628519
Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.
Kotze MJ, Langenhoven E, Retief AE, Seftel HC, Henderson HE, Weich HF., J. Med. Genet. 26(4), 1989
PMID: 2565980
Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia.
Schuster H, Stiefenhofer B, Wolfram G, Keller C, Humphries S, Huber A, Zollner N., Hum. Genet. 82(1), 1989
PMID: 2565869
The use of recombinant DNA techniques for the diagnosis of familial hypercholesterolaemia.
Humphries S, Taylor R, Jeenah M, Seed M., J. Inherit. Metab. Dis. 11 Suppl 1(), 1988
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TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.
Yamakawa K, Okafuji T, Iwamura Y, Yuzawa K, Satoh J, Hattori N, Yamanouchi Y, Yanagi H, Kawai K, Tsuchiya S., Hum. Genet. 80(1), 1988
PMID: 2901393

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