-
1
-
-
0025774523
-
A convenient multiplex PCR system for the detection of dystrophin gene deletions: A comparative analysis with cDNA hybridisation shows mistypings by both methods
-
Abbs, S., Yau, S.C., Clark, S. et al. (1991) 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., 28, 304-311.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 304-311
-
-
Abbs, S.1
Yau, S.C.2
Clark, S.3
-
2
-
-
0025244924
-
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
-
Beggs, A.H., Koenig, M., Boyce, F.M. and Kunkel, L.M. (1990) Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum. Genet., 86, 45-48.
-
(1990)
Hum. Genet.
, vol.86
, pp. 45-48
-
-
Beggs, A.H.1
Koenig, M.2
Boyce, F.M.3
Kunkel, L.M.4
-
3
-
-
0030043595
-
Skeletal, cardiac, and smooth muscle failure in Duchenne muscular dystrophy
-
Boland, B.J., Silbert, P.L., Groover, R.V. et al. (1996) Skeletal, cardiac, and smooth muscle failure in Duchenne muscular dystrophy. Pediat. Neurol., 14, 7-12.
-
(1996)
Pediat. Neurol.
, vol.14
, pp. 7-12
-
-
Boland, B.J.1
Silbert, P.L.2
Groover, R.V.3
-
4
-
-
0024245082
-
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
-
Chamberlain, J.S., Gibbs, R.A., Ranier, J.E. et al (1988) Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res., 9, 11141-11156.
-
(1988)
Nucleic Acids Res.
, vol.9
, pp. 11141-11156
-
-
Chamberlain, J.S.1
Gibbs, R.A.2
Ranier, J.E.3
-
5
-
-
0002503692
-
-
Innis, M., Gelfand, D. H., Sninsky, J. J. and White, T. J. (eds), Academic Press, San Diego
-
Chamberlain, J. S., Gibbs, R. A., Ranier, J. E., and Caskey, C. T. (1990) In Innis, M., Gelfand, D. H., Sninsky, J. J. and White, T. J. (eds), PCR Protocols: A guide to Methods and Applications. Academic Press, San Diego, pp. 272-281.
-
(1990)
PCR Protocols: A Guide to Methods and Applications
, pp. 272-281
-
-
Chamberlain, J.S.1
Gibbs, R.A.2
Ranier, J.E.3
Caskey, C.T.4
-
6
-
-
0026065749
-
Post-PCR sterilization: A method to control carryover contamination for the polymerase chain reaction
-
Cimino, G.D., Metchette, K.C., Tessman, J.W. et al. (1991) Post-PCR sterilization: a method to control carryover contamination for the polymerase chain reaction. Nucleic Acids Res., 19, 99-107.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 99-107
-
-
Cimino, G.D.1
Metchette, K.C.2
Tessman, J.W.3
-
7
-
-
0025943652
-
Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms
-
Clemens, P.R., Fenwick, R.G., Chamberlain, J.S., Gibbs, R.A. et al. (1991) Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am. J. Hum. Genet., 49, 951-960.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 951-960
-
-
Clemens, P.R.1
Fenwick, R.G.2
Chamberlain, J.S.3
Gibbs, R.A.4
-
8
-
-
0029061813
-
Simultaneous DNA 'fingerprinting', diagnosis of sex and single-gene defect status from single cells
-
Findlay, I., Urquhart, A., Quirke, P. et al. (1995) Simultaneous DNA 'fingerprinting', diagnosis of sex and single-gene defect status from single cells. Hum. Reprod., 10, 1005-1013.
-
(1995)
Hum. Reprod.
, vol.10
, pp. 1005-1013
-
-
Findlay, I.1
Urquhart, A.2
Quirke, P.3
-
9
-
-
0032753807
-
Analysis of five Duchenne muscular dystrophy exons and gender determination using conventional duplex polymerase chain reaction on single cells
-
Hussey, N.D., Donggui, H., Froiland, D.A. et al. (1999) Analysis of five Duchenne muscular dystrophy exons and gender determination using conventional duplex polymerase chain reaction on single cells. Mol. Hum. Reprod., 5, 1089-1094.
-
(1999)
Mol. Hum. Reprod.
, vol.5
, pp. 1089-1094
-
-
Hussey, N.D.1
Donggui, H.2
Froiland, D.A.3
-
10
-
-
0028240477
-
Preimplantation single cell analyses of dystrophin gene deletions
-
Kristjansson, K., Chong, S.S., Van den Veyver, I.B. et al. (1994) Preimplantation single cell analyses of dystrophin gene deletions. Nat. Genet., 6, 19-23.
-
(1994)
Nat. Genet.
, vol.6
, pp. 19-23
-
-
Kristjansson, K.1
Chong, S.S.2
Van Den Veyver, I.B.3
-
11
-
-
0031959726
-
Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis
-
Lee, S.H., Kwak, I.P., Cha, K.E. et al. (1998) Preimplantation diagnosis of non-deletion Duchenne muscular dystrophy (DMD) by linkage polymerase chain reaction analysis. Mol. Hum. Reprod., 4, 345-349.
-
(1998)
Mol. Hum. Reprod.
, vol.4
, pp. 345-349
-
-
Lee, S.H.1
Kwak, I.P.2
Cha, K.E.3
-
12
-
-
3242855896
-
-
Albelson, J.N. and Simon, M.I., (eds), Academic Press, New York
-
Li, H., Cui, X. and Arnheim, N. (1991) In Albelson, J.N. and Simon, M.I., (eds), Methods. A Companion to Methods in Enzymology. Academic Press, New York, pp. 49-59.
-
(1991)
Methods. A Companion to Methods in Enzymology
, pp. 49-59
-
-
Li, H.1
Cui, X.2
Arnheim, N.3
-
13
-
-
0028968665
-
Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletion
-
Liu, J., Lissens, W., Van Broeckhoven, C. et al. (1995) Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletion. Prenat. Diagn., 15, 351-358.
-
(1995)
Prenat. Diagn.
, vol.15
, pp. 351-358
-
-
Liu, J.1
Lissens, W.2
Van Broeckhoven, C.3
-
14
-
-
0025970931
-
A human X-Y homologous region encodes 'amelogenin'
-
Nakahori, Y., Takenaka, O. and Nakagome, Y. (1991) A human X-Y homologous region encodes 'amelogenin'. Genomics, 9, 264-269.
-
(1991)
Genomics
, vol.9
, pp. 264-269
-
-
Nakahori, Y.1
Takenaka, O.2
Nakagome, Y.3
-
15
-
-
0026877717
-
Use of modified nucleotides and uracil-DNA glycosylase (UNG) for the control of contamination in the PCR-based amplification of RNA
-
Pang, J., Modlin, J. and Yolken, R. (1992) Use of modified nucleotides and uracil-DNA glycosylase (UNG) for the control of contamination in the PCR-based amplification of RNA. Mol. Cell. Probes, 6, 251-256.
-
(1992)
Mol. Cell. Probes
, vol.6
, pp. 251-256
-
-
Pang, J.1
Modlin, J.2
Yolken, R.3
-
16
-
-
0029936083
-
Preimplantation genetic diagnosis of β-thalassaemia major
-
Ray P.F., Kaeda J.S., Bingham, J. et al. (1996a) Preimplantation genetic diagnosis of β-thalassaemia major. Lancet, 347, 1696.
-
(1996)
Lancet
, vol.347
, pp. 1696
-
-
Ray, P.F.1
Kaeda, J.S.2
Bingham, J.3
-
17
-
-
0030089526
-
Increasing the denaturation temperature during the first cycles of nested amplification reduces allele dropout from single cells for preimplantation genetic diagnosis
-
Ray, P.F. and Handyside, A.H. (1996b) Increasing the denaturation temperature during the first cycles of nested amplification reduces allele dropout from single cells for preimplantation genetic diagnosis. Mol. Hum, Reprod., 2, 213-218.
-
(1996)
Mol. Hum, Reprod.
, vol.2
, pp. 213-218
-
-
Ray, P.F.1
Handyside, A.H.2
-
18
-
-
0034513788
-
First specific preimplantation genetic diagnosis (PGD) for ornithine transcarbamylase deficiency
-
Ray P.F., Gigarel, N., Bonnefont, J.P. et al. (2000) First specific preimplantation genetic diagnosis (PGD) for ornithine transcarbamylase deficiency. Prenat. Diagn., 20, 1048-1054.
-
(2000)
Prenat. Diagn.
, vol.20
, pp. 1048-1054
-
-
Ray, P.F.1
Gigarel, N.2
Bonnefont, J.P.3
-
19
-
-
0032439813
-
Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the Δ508 deletion causing cystic fibrosis in a clinical practice
-
Ray, P.F., Winston, R.M.L.and Handyside, A.H. (1998) Assessment of the reliability of single blastomere analysis for preimplantation diagnosis of the Δ508 deletion causing cystic fibrosis in a clinical practice. Prenat. Diagn., 18, 1402-1412.
-
(1998)
Prenat. Diagn.
, vol.18
, pp. 1402-1412
-
-
Ray, P.F.1
Winston, R.M.L.2
Handyside, A.H.3
-
20
-
-
0023741379
-
Patterns of exon deletions in Duchenne and Becker muscular dystrophy
-
Read, A.P., Mountford, R.C., Forrest, S.M. et al. (1988) Patterns of exon deletions in Duchenne and Becker muscular dystrophy. Hum. Genet., 80, 152-156.
-
(1988)
Hum. Genet.
, vol.80
, pp. 152-156
-
-
Read, A.P.1
Mountford, R.C.2
Forrest, S.M.3
-
21
-
-
0028837312
-
The human dystrophin gene requires 16 h to be transcribed and is cotranscriptionally spliced
-
Tennyson, C.N., Klamut, H.J. and Worton, R.G. (1995) The human dystrophin gene requires 16 h to be transcribed and is cotranscriptionally spliced. Nature Genet., 9, 184-190.
-
(1995)
Nature Genet.
, vol.9
, pp. 184-190
-
-
Tennyson, C.N.1
Klamut, H.J.2
Worton, R.G.3
-
22
-
-
0026800930
-
Utilizing uracil DNA glycosylase to control carryover contamination in PCR: Characterization of residual UDG activity following thermal cycling
-
Thomton, C.G., Hartley, J.L. and Rashtchian, A. (1992) Utilizing uracil DNA glycosylase to control carryover contamination in PCR: characterization of residual UDG activity following thermal cycling. Biotechniques, 13, 180-184.
-
(1992)
Biotechniques
, vol.13
, pp. 180-184
-
-
Thomton, C.G.1
Hartley, J.L.2
Rashtchian, A.3
-
23
-
-
0027267988
-
Use of PCR primers containing a 3′-terminal ribose residue to prevent cross-contamination of amplified sequences
-
Walder, R.Y., Hayes, J.R. and Walder, J.A. (1993) Use of PCR primers containing a 3′-terminal ribose residue to prevent cross-contamination of amplified sequences. Nucleic Acids Res., 21, 4339-4343.
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 4339-4343
-
-
Walder, R.Y.1
Hayes, J.R.2
Walder, J.A.3
-
24
-
-
0026865024
-
Preferential PCR amplification of alleles: Mechanisms and solutions
-
Walsh, P.S., Erlich, H.A. and Higuchi, R. (1992) Preferential PCR amplification of alleles: mechanisms and solutions. PCR Methods Appl., 1, 241-250.
-
(1992)
PCR Methods Appl.
, vol.1
, pp. 241-250
-
-
Walsh, P.S.1
Erlich, H.A.2
Higuchi, R.3
-
25
-
-
0026755807
-
Whole genome amplification from a single cell: Implications for genetic analysis
-
Zhang, L., Cui, X., Schmitt, K. et al. (1992) Whole genome amplification from a single cell: implications for genetic analysis. Proc. Natl Acad. Sci. USA, 89, 5847-5851.
-
(1992)
Proc. Natl Acad. Sci. USA
, vol.89
, pp. 5847-5851
-
-
Zhang, L.1
Cui, X.2
Schmitt, K.3
|