-
1
-
-
19944407550
-
Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR. Assessment on 18,000 consecutive clinical samples
-
Cirigliano V, Voglino G, Canadas MP, et al. 2004. Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR. Assessment on 18,000 consecutive clinical samples. Mol Hum Reprod 10: 839-846.
-
(2004)
Mol Hum Reprod
, vol.10
, pp. 839-846
-
-
Cirigliano, V.1
Voglino, G.2
Canadas, M.P.3
-
2
-
-
0031925460
-
Rapid trisomy diagnosis (21, 18, and 13) using fluorescent PCR and short tandem repeats: Applications for prenatal diagnosis and preimplantation genetic diagnosis
-
Findlay I, Toth T, Matthews P, Marton T, Quirke P, Papp Z. 1998. Rapid trisomy diagnosis (21, 18, and 13) using fluorescent PCR and short tandem repeats: applications for prenatal diagnosis and preimplantation genetic diagnosis. J Assist Reprod Genet 15: 266-275.
-
(1998)
J Assist Reprod Genet
, vol.15
, pp. 266-275
-
-
Findlay, I.1
Toth, T.2
Matthews, P.3
Marton, T.4
Quirke, P.5
Papp, Z.6
-
3
-
-
0037220006
-
A novel rapid single nucleotide polymorphism (SNP)-based method for assessment of hematopoietic chimerism after allogeneic stem cell transplantation
-
Hochberg EP, Miklos DB, Neuberg D, et al. 2003. A novel rapid single nucleotide polymorphism (SNP)-based method for assessment of hematopoietic chimerism after allogeneic stem cell transplantation. Blood 101: 363-369.
-
(2003)
Blood
, vol.101
, pp. 363-369
-
-
Hochberg, E.P.1
Miklos, D.B.2
Neuberg, D.3
-
4
-
-
0035865322
-
A map of human genome sequence variations containing 1.42 million single nucleotide polymorphisms
-
The International SNP Map Working Group. 2001. A map of human genome sequence variations containing 1.42 million single nucleotide polymorphisms. Nature 409: 928-933.
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
-
5
-
-
0031697439
-
Reading of bits of genetic information: Methods for single-nucleotide polymorphism analysis
-
Landegren U, Nilsson M, Kwok P-Y. 1998. Reading of bits of genetic information: methods for single-nucleotide polymorphism analysis. Genome Res 8: 769-776.
-
(1998)
Genome Res
, vol.8
, pp. 769-776
-
-
Landegren, U.1
Nilsson, M.2
Kwok, P.-Y.3
-
6
-
-
0035060502
-
DNA melting analysis for detection of single nucleotide polymorphisms
-
Lipsky RH, Mazzanti CM, Rudolph JG, et al. 2001. DNA melting analysis for detection of single nucleotide polymorphisms. Clin Chem 47: 635-644.
-
(2001)
Clin Chem
, vol.47
, pp. 635-644
-
-
Lipsky, R.H.1
Mazzanti, C.M.2
Rudolph, J.G.3
-
7
-
-
0035559697
-
Mutation detection using fluorescent hybridization probes and melting curve analysis
-
Lyon E. 2001. Mutation detection using fluorescent hybridization probes and melting curve analysis. Expert Rev Mol Diagn 1: 92-101.
-
(2001)
Expert Rev Mol Diagn
, vol.1
, pp. 92-101
-
-
Lyon, E.1
-
8
-
-
7744225371
-
Strategies for the rapid prenatal diagnosis of chromosome aneuploidy
-
Mann K, Donaghue C, Fox SP, Docherty Z, Ogilvie CM. 2004. Strategies for the rapid prenatal diagnosis of chromosome aneuploidy. Eur J Hum Genet 12: 907-915.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 907-915
-
-
Mann, K.1
Donaghue, C.2
Fox, S.P.3
Docherty, Z.4
Ogilvie, C.M.5
-
9
-
-
0342699648
-
Apolipoprotein E allele distribution in trisomy 13, 18, and 21 conceptuses in a Hungarian population
-
Nagy B, Ban Z, Toth-Pal E, Papp C, Fintor L, Papp Z. 2000. Apolipoprotein E allele distribution in trisomy 13, 18, and 21 conceptuses in a Hungarian population. Am J Clin Pathol 113: 535-538.
-
(2000)
Am J Clin Pathol
, vol.113
, pp. 535-538
-
-
Nagy, B.1
Ban, Z.2
Toth-Pal, E.3
Papp, C.4
Fintor, L.5
Papp, Z.6
-
10
-
-
0038272057
-
Rapid detection of aneuploidy (trisomy 21) by allele quantification combined with melting curve analysis of single-nucleotide polymorphism loci
-
Pont-Kingdon G, Lyon E. 2003. Rapid detection of aneuploidy (trisomy 21) by allele quantification combined with melting curve analysis of single-nucleotide polymorphism loci. Clin Chem 49: 1087-1094.
-
(2003)
Clin Chem
, vol.49
, pp. 1087-1094
-
-
Pont-Kingdon, G.1
Lyon, E.2
-
11
-
-
2642709215
-
Prenatal detection of trisomy 13 from amniotic fluid by quantitative fluorescent polymerase chain reaction
-
Toth T, Findlay I, Papp C, et al. 1998a. Prenatal detection of trisomy 13 from amniotic fluid by quantitative fluorescent polymerase chain reaction. Prenat Diagn 18: 669-674.
-
(1998)
Prenat Diagn
, vol.18
, pp. 669-674
-
-
Toth, T.1
Findlay, I.2
Papp, C.3
-
12
-
-
0031980021
-
Prenatal detection of trisomy 21 and 18 from amniotic fluid by quantitative fluorescent polymerase chain reaction
-
Toth T, Findlay I, Papp C, et al. 1998b. Prenatal detection of trisomy 21 and 18 from amniotic fluid by quantitative fluorescent polymerase chain reaction. J Med Genet 35: 126-129.
-
(1998)
J Med Genet
, vol.35
, pp. 126-129
-
-
Toth, T.1
Findlay, I.2
Papp, C.3
|