-
1
-
-
0028290955
-
New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines
-
Banchs I, Bosch A, Guimera J, Lazaro C, Puig A, Estivill X (1994) New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines. Hum Mutat 3:365-372
-
(1994)
Hum Mutat
, vol.3
, pp. 365-372
-
-
Banchs, I.1
Bosch, A.2
Guimera, J.3
Lazaro, C.4
Puig, A.5
Estivill, X.6
-
2
-
-
0028224645
-
Mutator phenotypes in human colorectal carcinoma cell lines
-
Bhattacharyya NP, Skandalis A, Ganesh A, Groden J, Meuth M (1994) Mutator phenotypes in human colorectal carcinoma cell lines. Proc Natl Acad Sci U S A 91:6319-6323
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 6319-6323
-
-
Bhattacharyya, N.P.1
Skandalis, A.2
Ganesh, A.3
Groden, J.4
Meuth, M.5
-
3
-
-
0034789823
-
Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies
-
Cirigliano V, Ejarque M, Canadas MP, Lloveras E, Plaja A, Perez MM, Fuster C, Egozcue J (2001) Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies. Mol Hum Reprod 7:1001-1006
-
(2001)
Mol Hum Reprod
, vol.7
, pp. 1001-1006
-
-
Cirigliano, V.1
Ejarque, M.2
Canadas, M.P.3
Lloveras, E.4
Plaja, A.5
Perez, M.M.6
Fuster, C.7
Egozcue, J.8
-
4
-
-
0034079715
-
Heterogeneous mutation processes in human microsatellite DNA sequences
-
Ellegren H (2000) Heterogeneous mutation processes in human microsatellite DNA sequences. Nat Genet 24:400-402
-
(2000)
Nat Genet
, vol.24
, pp. 400-402
-
-
Ellegren, H.1
-
5
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov Y, Peinado MA, Malkhosyan S, Shibata D, Perucho M (1993) Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature 363:558-561
-
(1993)
Nature
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkhosyan, S.3
Shibata, D.4
Perucho, M.5
-
7
-
-
0037228362
-
The mutational spectrum of human autosomal tetranucleotide microsatellites
-
Leopoldino A, Pena S (2002) The mutational spectrum of human autosomal tetranucleotide microsatellites. Hum Mutat 21-71-79
-
(2002)
Hum Mutat
, vol.21
, pp. 71-79
-
-
Leopoldino, A.1
Pena, S.2
-
8
-
-
0023256559
-
Slipped-strand mispairing: A major mechanism for DNA sequence evolution
-
Levinson G, Gutman GA (1987) Slipped-strand mispairing: A major mechanism for DNA sequence evolution. Mol Biol Evol 4:203-221
-
(1987)
Mol Biol Evol
, vol.4
, pp. 203-221
-
-
Levinson, G.1
Gutman, G.A.2
-
9
-
-
0035968604
-
Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis
-
Mann K, Fox SP, Abbs SJ, Yau SC, Scriven PN, Docherty Z, Ogilvie CM (2001) Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis. Lancet 358:1057-1061
-
(2001)
Lancet
, vol.358
, pp. 1057-1061
-
-
Mann, K.1
Fox, S.P.2
Abbs, S.J.3
Yau, S.C.4
Scriven, P.N.5
Docherty, Z.6
Ogilvie, C.M.7
-
10
-
-
0029061638
-
Mismatch repair deficiency in phenotypically normal human cells
-
Parsons R, Li GM, Longley M, Modrich P, Liu B, Berk T, Hamilton SR, Kinzler KW, Vogelstein B (1995) Mismatch repair deficiency in phenotypically normal human cells. Science 268:738-740
-
(1995)
Science
, vol.268
, pp. 738-740
-
-
Parsons, R.1
Li, G.M.2
Longley, M.3
Modrich, P.4
Liu, B.5
Berk, T.6
Hamilton, S.R.7
Kinzler, K.W.8
Vogelstein, B.9
-
11
-
-
0032904353
-
Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: First application on 247 chorionic villus samples
-
Pertl B, Kopp S, Kroisel PM, Tului L, Brambati B, Adinolfi M (1999) Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: First application on 247 chorionic villus samples. J Med Genet 36:300-303
-
(1999)
J Med Genet
, vol.36
, pp. 300-303
-
-
Pertl, B.1
Kopp, S.2
Kroisel, P.M.3
Tului, L.4
Brambati, B.5
Adinolfi, M.6
-
12
-
-
0033841101
-
Detection of aneuploidy in chromosomes X, Y, 13, 18 and 21 by QF-PCR in 662 selected pregnancies at risk
-
Schmidt W, Jenderny J, Hecher K, Hackeloer BJ, Kerber S, Kochhan L, Held KR (2000) Detection of aneuploidy in chromosomes X, Y, 13, 18 and 21 by QF-PCR in 662 selected pregnancies at risk. Mol Hum Reprod 6:855-860
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 855-860
-
-
Schmidt, W.1
Jenderny, J.2
Hecher, K.3
Hackeloer, B.J.4
Kerber, S.5
Kochhan, L.6
Held, K.R.7
-
13
-
-
0028362325
-
Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation
-
Shibata D, Peinado MA, Ionov Y, Malkhosyan S, Perucho M (1994) Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation. Nat Genet 6:273-281
-
(1994)
Nat Genet
, vol.6
, pp. 273-281
-
-
Shibata, D.1
Peinado, M.A.2
Ionov, Y.3
Malkhosyan, S.4
Perucho, M.5
-
14
-
-
0035360278
-
Extensive somatic microsatellite mutations in normal human tissue
-
Vilkki S, Tsao JL, Loukola A, Poyhonen M, Vierimaa O, Herva R, Aaltonen LA, Shibata D (2001) Extensive somatic microsatellite mutations in normal human tissue. Cancer Res 61:4541-4544
-
(2001)
Cancer Res
, vol.61
, pp. 4541-4544
-
-
Vilkki, S.1
Tsao, J.L.2
Loukola, A.3
Poyhonen, M.4
Vierimaa, O.5
Herva, R.6
Aaltonen, L.A.7
Shibata, D.8
-
15
-
-
0027161022
-
Mutation of human short tandem repeats
-
Weber JL, Wong C (1993) Mutation of human short tandem repeats. Hum Mol Genet 2:1123-1128
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1123-1128
-
-
Weber, J.L.1
Wong, C.2
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