-
1
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson, S., A.T. Bankier, B.G. Barrell, M.H.L. de Bruijn, A.R. Coulson, J. Drouin, I.C. Eperon, D.P. Nierlich et al. 1981. Sequence and organization of the human mitochondrial genome. Nature 290:457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
De Bruijn, M.H.L.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
-
2
-
-
0024316973
-
Detection of specific DNa sequences by fluorescent amplification: A color complementation assay
-
Chehab, F.F. and Y.W. Kan. 1989. Detection of specific DNA sequences by fluorescent amplification: a color complementation assay. Proc. Natl. Acad. Sci. USA 86:9178-9182.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 9178-9182
-
-
Chehab, F.F.1
Kan, Y.W.2
-
3
-
-
0026900908
-
Fluorescence-based, muliplex allele-specific PCR (MASPCR) detection of the dF508 deletion in the cystic tibrosis transmembrane conductance regulator (CFTR) gene
-
Fortina, P., R. Conant, T. Parrella, E. Rappaport, T. Scanlin, E. Schwartz, J.M. Robertson and S. Surrey. 1992 Fluorescence-based, muliplex allele-specific PCR (MASPCR) detection of the dF508 deletion in the cystic tibrosis transmembrane conductance regulator (CFTR) gene. Mol. Cell. Probes 6:353-356.
-
(1992)
Mol. Cell. Probes
, vol.6
, pp. 353-356
-
-
Fortina, P.1
Conant, R.2
Parrella, T.3
Rappaport, E.4
Scanlin, T.5
Schwartz, E.6
Robertson, J.M.7
Surrey, S.8
-
4
-
-
0024524650
-
Detection of DNA base differences by competitive oligonucleotide priming
-
Gibbs, R.A., P.N. Nguyen and C.T. Caskey. 1989. Detection of DNA base differences by competitive oligonucleotide priming. Nucleic Acids Res. 17:2437-2448.
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 2437-2448
-
-
Gibbs, R.A.1
Nguyen, P.N.2
Caskey, C.T.3
-
5
-
-
0025910614
-
A new mtDNA mutation associated with Leber hereditary optic neuropathy
-
Huoponen, K., J. Vilkki, P. Aula, E.K. Nikoskelainen and M.L. Savontaus. 1991. A new mtDNA mutation associated with Leber hereditary optic neuropathy. Am. J. Hum. Genet. 48:1147-1153.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 1147-1153
-
-
Huoponen, K.1
Vilkki, J.2
Aula, P.3
Nikoskelainen, E.K.4
Savontaus, M.L.5
-
6
-
-
0026757115
-
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
-
Johns, D.R., M.J. Neufeld and R.D. Park. 1992. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy. Biochem. Biophys. Res. Commun. 187:1551-1557.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.187
, pp. 1551-1557
-
-
Johns, D.R.1
Neufeld, M.J.2
Park, R.D.3
-
7
-
-
0025297178
-
Direct electrophoretic detection of the allele state of single DNA molecules in human sperm by using the polymerase chain reaction
-
Li, H., X. Cui and N. Arnheim. 1990. Direct electrophoretic detection of the allele state of single DNA molecules in human sperm by using the polymerase chain reaction. Proc. Natl. Acad. Sci. USA 87:4580-4584.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 4580-4584
-
-
Li, H.1
Cui, X.2
Arnheim, N.3
-
8
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S.A., D.D. Dykes and H.F. Polesky. 1988. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16:1215.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
9
-
-
0023022499
-
Analysis of enzymatically amplified β-globin and HLA-DQ DNA with allele-specific oligonucleotide probes
-
Saiki, R.K., T.L. Bugawan, G.T. Horn, K.B. Mullis and H.A. Erlich. 1986. Analysis of enzymatically amplified β-globin and HLA-DQ DNA with allele-specific oligonucleotide probes. Nature 324:163-166.
-
(1986)
Nature
, vol.324
, pp. 163-166
-
-
Saiki, R.K.1
Bugawan, T.L.2
Horn, G.T.3
Mullis, K.B.4
Erlich, H.A.5
-
10
-
-
0001442557
-
Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes
-
Saiki, R.K., P.S. Walsh and D.H. Levinson. 1989. Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes. Proc. Natl. Acad. Sci. USA 86:6230-6234.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 6230-6234
-
-
Saiki, R.K.1
Walsh, P.S.2
Levinson, D.H.3
-
11
-
-
0025650533
-
A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E
-
Syvänen, A.-C., K. Aalto-Setälä, L. Harju, K. Kontula and H. Söderlund. 1990. A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E. Genomics 8:684-692.
-
(1990)
Genomics
, vol.8
, pp. 684-692
-
-
Syvänen, A.-C.1
Aalto-Setälä, K.2
Harju, L.3
Kontula, K.4
Söderlund, H.5
-
12
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace, D.C., G. Singh, M.T. Lott, J.A. Hodge, T.G. Schurr, A.M.S. Lezza, L.J. Elsas and E.K. Nikoskelainen. 1988. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 242:1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.S.6
Elsas, L.J.7
Nikoskelainen, E.K.8
-
13
-
-
0002713231
-
Allele-specific enzymatic amplification of β-globin genomic DNA for the diagnosis of sickle cell anemia
-
Wu, D.Y., L. Ugozzoli, B.K. Pal and R.B. Wallace. 1989. Allele-specific enzymatic amplification of β-globin genomic DNA for the diagnosis of sickle cell anemia. Proc. Natl. Acad. Sci. USA 86:2757-2760.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 2757-2760
-
-
Wu, D.Y.1
Ugozzoli, L.2
Pal, B.K.3
Wallace, R.B.4
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