Markham AF - Search Results

1

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

Newton CR, Graham A, Heptinstall LE, Powell SJ, Summers C, Kalsheker N, Smith JC, Markham AF. Newton CR, et al. Among authors: markham af. Nucleic Acids Res. 1989 Apr 11;17(7):2503-16. doi: 10.1093/nar/17.7.2503. Nucleic Acids Res. 1989. PMID: 2785681 Free PMC article.

2

The production of PCR products with 5' single-stranded tails using primers that incorporate novel phosphoramidite intermediates.

Newton CR, Holland D, Heptinstall LE, Hodgson I, Edge MD, Markham AF, McLean MJ. Newton CR, et al. Among authors: markham af. Nucleic Acids Res. 1993 Mar 11;21(5):1155-62. doi: 10.1093/nar/21.5.1155. Nucleic Acids Res. 1993. PMID: 8464700 Free PMC article.

3

Direct haplotype determination by double ARMS: specificity, sensitivity and genetic applications.

Lo YM, Patel P, Newton CR, Markham AF, Fleming KA, Wainscoat JS. Lo YM, et al. Among authors: markham af. Nucleic Acids Res. 1991 Jul 11;19(13):3561-7. doi: 10.1093/nar/19.13.3561. Nucleic Acids Res. 1991. PMID: 1852606 Free PMC article.

4

Molecular characterisation of two alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) Null(Newport) (Gly115----Ser) and (Pi) Z Wrexham (Ser-19----Leu).

Graham A, Kalsheker NA, Bamforth FJ, Newton CR, Markham AF. Graham A, et al. Among authors: markham af. Hum Genet. 1990 Oct;85(5):537-40. doi: 10.1007/BF00194233. Hum Genet. 1990. PMID: 2227940

5

Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant.

Graham A, Hayes K, Weidinger S, Newton CR, Markham AF, Kalsheker NA. Graham A, et al. Among authors: markham af. Hum Genet. 1990 Aug;85(3):381-2. doi: 10.1007/BF00206766. Hum Genet. 1990. PMID: 2394452

6

Nucleotide sequence of cDNA for human aldose reductase.

Graham A, Hedge PJ, Powell SJ, Riley J, Brown L, Gammack A, Carey F, Markham AF. Graham A, et al. Among authors: markham af. Nucleic Acids Res. 1989 Oct 25;17(20):8368. doi: 10.1093/nar/17.20.8368. Nucleic Acids Res. 1989. PMID: 2510130 Free PMC article. No abstract available.

7

Amplification refractory mutation system for prenatal diagnosis and carrier assessment in cystic fibrosis.

Newton CR, Heptinstall LE, Summers C, Super M, Schwarz M, Anwar R, Graham A, Smith JC, Markham AF. Newton CR, et al. Among authors: markham af. Lancet. 1989 Dec 23-30;2(8678-8679):1481-3. doi: 10.1016/s0140-6736(89)92931-0. Lancet. 1989. PMID: 2574768

8

Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256----Val); PiMmalton (Phe51----deletion) and PiI (Arg39----Cys).

Graham A, Kalsheker NA, Newton CR, Bamforth FJ, Powell SJ, Markham AF. Graham A, et al. Among authors: markham af. Hum Genet. 1989 Dec;84(1):55-8. doi: 10.1007/BF00210671. Hum Genet. 1989. PMID: 2606478

9

Rapid determination of DNA concentration in multiple samples.

Riley J, Jenner D, Smith JC, Markham AF. Riley J, et al. Among authors: markham af. Nucleic Acids Res. 1989 Oct 25;17(20):8383. doi: 10.1093/nar/17.20.8383. Nucleic Acids Res. 1989. PMID: 2813073 Free PMC article. No abstract available.

10

Diagnosis of alpha 1-antitrypsin deficiency by enzymatic amplification of human genomic DNA and direct sequencing of polymerase chain reaction products.

Newton CR, Kalsheker N, Graham A, Powell S, Gammack A, Riley J, Markham AF. Newton CR, et al. Among authors: markham af. Nucleic Acids Res. 1988 Sep 12;16(17):8233-43. doi: 10.1093/nar/16.17.8233. Nucleic Acids Res. 1988. PMID: 3262215 Free PMC article.

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