Literature DB >> 2294422

Genotyping errors with the polymerase chain reaction.

F K Fujimura, H Northrup, A L Beaudet, W E O'Brien.   

Abstract

Mesh：

Year:  1990        PMID： 2294422     DOI： 10.1056/NEJM199001043220117

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  10 in total

1.  Novel amplification of DNA in a hairpin structure: towards a radical elimination of PCR errors from amplified DNA.

Authors:  Manjit Kaur; G Mike Makrigiorgos
Journal:  Nucleic Acids Res       Date:  2003-03-15       Impact factor: 16.971

2.  In vitro gene amplification for prenatal diagnosis of congenital adrenal hyperplasia.

Authors:  G Rumsby; J W Honour
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

3.  A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.

Authors:  S Abbs; S C Yau; S Clark; C G Mathew; M Bobrow
Journal:  J Med Genet       Date:  1991-05       Impact factor: 6.318

4.  Influence of mosaicism on sexing of human preembryos detected by the polymerase chain reaction.

Authors:  Y Katagiri; S Katayama
Journal:  J Assist Reprod Genet       Date:  1996-08       Impact factor: 3.412

5.  A region of primer binding variation at the D6S265 locus associated with HLA-A25 and HLA-A26 antigens.

Authors:  W Pyper; M Burt; L Powell; S Webb; L Adès; J Halliday; E Jazwinska
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

6.  Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.

Authors:  S C Yau; M Bobrow; C G Mathew; S J Abbs
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

7.  A third mutation at the CpG dinucleotide of codon 504 and a silent mutation at codon 506 of the HEX A gene.

Authors:  B H Paw; L C Wood; E F Neufeld
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

8.  Benign missense variations in the cystic fibrosis gene.

Authors:  K Kobayashi; M R Knowles; R C Boucher; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

Review 9.  Separating measurement and expression models clarifies confusion in single-cell RNA sequencing analysis.

Authors:  Abhishek Sarkar; Matthew Stephens
Journal:  Nat Genet       Date:  2021-05-24       Impact factor: 38.330

10.  Targeted sequencing identifies novel variants in common and rare MODY genes.

Authors:  Lucas S de Santana; Lilian A Caetano; Aline D Costa-Riquetto; Pedro C Franco; Renata P Dotto; André F Reis; Letícia S Weinert; Sandra P Silveiro; Marcio F Vendramini; Flaviene A do Prado; Giovanna C P Abrahão; Ana Gregória F P de Almeida; Maria da G Rodrigues Tavares; Wagner Rodrigo B Gonçalves; Augusto C Santomauro Junior; Bruno Halpern; Alexander A L Jorge; Marcia Nery; Milena G Teles
Journal:  Mol Genet Genomic Med       Date:  2019-10-08       Impact factor: 2.183
  10 in total

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