G to A Polymorphism in the Second Exon of the BCL2 Gene
Overview
Overview
Journal
Nucleic Acids Res
Publisher
Oxford University Press
Specialty
Biochemistry
Date
1991 Apr 25
PMID
2030986
Citations
3
Authors
Affiliations
Affiliations
Soon will be listed here.
Citing Articles
Syvanen A, Sajantila A, Lukka M Am J Hum Genet. 1993; 52(1):46-59.
PMID: 8434605 PMC: 1682118.
Nolte M, Werner M, Spann W, Schnabel B, von Wasielewski R, Wilkens L Virchows Arch. 1995; 426(1):37-41.
PMID: 7704322 DOI: 10.1007/BF00194696.
Louie D, Kant J, Brooks J, Reed J Am J Pathol. 1991; 139(6):1231-7.
PMID: 1750500 PMC: 1886479.
References
1.
Montandon A, Green P, Giannelli F, Bentley D
. Direct detection of point mutations by mismatch analysis: application to haemophilia B. Nucleic Acids Res. 1989; 17(9):3347-58.
PMC: 317779.
DOI: 10.1093/nar/17.9.3347.
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2.
Ohara O, Dorit R, Gilbert W
. One-sided polymerase chain reaction: the amplification of cDNA. Proc Natl Acad Sci U S A. 1989; 86(15):5673-7.
PMC: 297692.
DOI: 10.1073/pnas.86.15.5673.
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3.
Phaneuf D, Labelle Y, Berube D, Arden K, Cavenee W, Gagne R
. Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15. Am J Hum Genet. 1991; 48(3):525-35.
PMC: 1682993.
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4.
Tanguay R, Valet J, Lescault A, Duband J, Laberge C, Lettre F
. Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I). Am J Hum Genet. 1990; 47(2):308-16.
PMC: 1683717.
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5.
Grandchamp B, Picat C, de Rooij F, Beaumont C, Wilson P, Deybach J
. A point mutation G----A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria. Nucleic Acids Res. 1989; 17(16):6637-49.
PMC: 318356.
DOI: 10.1093/nar/17.16.6637.
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