Genotyping errors with the polymerase chain reaction
- PMID: 2294422
- DOI: 10.1056/NEJM199001043220117
Genotyping errors with the polymerase chain reaction
Similar articles
-
[Detection of Delta-F508 mutation by PCR (polymerase chain reaction) in patients with cystic fibrosis].An Esp Pediatr. 1993 Dec;39(6):557-8. An Esp Pediatr. 1993. PMID: 8166420 Spanish. No abstract available.
-
Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactions.Mol Biol Med. 1990 Aug;7(4):359-64. Mol Biol Med. 1990. PMID: 1978221
-
[Interference of P1290 P polymorphism (4002 A--> G) in molecular diagnosis of mucoviscidosis using the cystic fibrosis assay: an example of a diagnostic trap].Ann Biol Clin (Paris). 1999 Nov-Dec;57(6):741-2. Ann Biol Clin (Paris). 1999. PMID: 10572229 French. No abstract available.
-
[Oligonucleotide-genotyping of the HLA-DRB gene after enzymatic amplification by polymerase chain reaction].Tanpakushitsu Kakusan Koso. 1989 Dec;34(15):1989-2002. Tanpakushitsu Kakusan Koso. 1989. PMID: 2575264 Review. Japanese. No abstract available.
-
[Diagnosis of cystic fibrosis; simple genotyping to rule out the disease preferable to starting with the sweat test].Ned Tijdschr Geneeskd. 2003 May 24;147(21):1001-5. Ned Tijdschr Geneeskd. 2003. PMID: 12811969 Review. Dutch.
Cited by
-
Separating measurement and expression models clarifies confusion in single-cell RNA sequencing analysis.Nat Genet. 2021 Jun;53(6):770-777. doi: 10.1038/s41588-021-00873-4. Epub 2021 May 24. Nat Genet. 2021. PMID: 34031584 Free PMC article. Review.
-
A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.J Med Genet. 1991 May;28(5):304-11. doi: 10.1136/jmg.28.5.304. J Med Genet. 1991. PMID: 1865467 Free PMC article.
-
Influence of mosaicism on sexing of human preembryos detected by the polymerase chain reaction.J Assist Reprod Genet. 1996 Aug;13(7):586-91. doi: 10.1007/BF02066613. J Assist Reprod Genet. 1996. PMID: 8844317
-
A third mutation at the CpG dinucleotide of codon 504 and a silent mutation at codon 506 of the HEX A gene.Am J Hum Genet. 1991 Jun;48(6):1139-46. Am J Hum Genet. 1991. PMID: 1827944 Free PMC article.
-
In vitro gene amplification for prenatal diagnosis of congenital adrenal hyperplasia.J Med Genet. 1990 Nov;27(11):676-8. doi: 10.1136/jmg.27.11.676. J Med Genet. 1990. PMID: 2277381 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources