-
1
-
-
0012459519
-
-
Prepared by the American Association of Blood Banks Parentage Testing Standards Program Unit
-
AABB. 1999. Annual report summary for 1999. Prepared by the American Association of Blood Banks Parentage Testing Standards Program Unit. www.promega.com/geneticidproc/ussymp11proc/paternity_minisymp/baird.pdf.
-
(1999)
Annual Report Summary for 1999
-
-
-
2
-
-
0033854335
-
The ancestry of Brazilian mtDNA lineages
-
Alves-Silva J, da Silva Santos M, Guimaraes PE, Ferreira AC, Bandelt HJ, Pena SD, Prado VE 2000. The ancestry of Brazilian mtDNA lineages. Am J Hum Genet 67:444-461.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 444-461
-
-
Alves-Silva, J.1
Da Silva Santos, M.2
Guimaraes, P.E.3
Ferreira, A.C.4
Bandelt, H.J.5
Pena, S.D.6
Prado, V.E.7
-
3
-
-
0026865348
-
Tetranucleotide repeat polymorphism at the human thyroid peroxidase (hTPO) locus
-
Anker R, Steinbrueck T, Donis-Keller H. 1992. Tetranucleotide repeat polymorphism at the human thyroid peroxidase (hTPO) locus. Hum Mol Genet 1:137.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 137
-
-
Anker, R.1
Steinbrueck, T.2
Donis-Keller, H.3
-
4
-
-
0034326305
-
Sequence interruptions confer differential stability at microsatellite alleles in repair-deficient cells
-
Bacon AL, Farrington SM, Dunlop MG. 2000. Sequence interruptions confer differential stability at microsatellite alleles in repair-deficient cells. Hum Mol Genet 9:2707-2713.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2707-2713
-
-
Bacon, A.L.1
Farrington, S.M.2
Dunlop, M.G.3
-
5
-
-
0028184174
-
High resolution of human evolutionary trees with polymorphic microsatellites
-
Bowcock AM, Ruiz-Linares A, Tomfohrde J, Minch E, Kidd JR, Cavalli-Sforza LL. 1994. High resolution of human evolutionary trees with polymorphic microsatellites. Nature 368:455-457.
-
(1994)
Nature
, vol.368
, pp. 455-457
-
-
Bowcock, A.M.1
Ruiz-Linares, A.2
Tomfohrde, J.3
Minch, E.4
Kidd, J.R.5
Cavalli-Sforza, L.L.6
-
6
-
-
0031778070
-
Mutation rate in human microsatellites: Influence of the structure and length of the tandem repeat
-
Brinkmann B, Klintschar M, Neuhuber F, Huhne J, Rolf B. 1998. Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am J Hum Genet 62:1408-1415.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1408-1415
-
-
Brinkmann, B.1
Klintschar, M.2
Neuhuber, F.3
Huhne, J.4
Rolf, B.5
-
8
-
-
0032766235
-
Divergent human Y-chromosome microsatellite evolution rates
-
Carvalho-Silva DR, Santos FR, Hutz MH, Salzano FM, Pena SD. 1999. Divergent human Y-chromosome microsatellite evolution rates. J Mol Evol 49:204-214.
-
(1999)
J Mol Evol
, vol.49
, pp. 204-214
-
-
Carvalho-Silva, D.R.1
Santos, F.R.2
Hutz, M.H.3
Salzano, F.M.4
Pena, S.D.5
-
10
-
-
0029971170
-
Paternity exclusion by DNA markers: Effects of paternal mutations
-
Chakraborty R, Stivers DN. 1996. Paternity exclusion by DNA markers: effects of paternal mutations. J Forensic Sci 41: 671-677.
-
(1996)
J Forensic Sci
, vol.41
, pp. 671-677
-
-
Chakraborty, R.1
Stivers, D.N.2
-
11
-
-
0030570421
-
Estimation of mutation rates from parentage exclusion data: Applications to STR and VNTR loci
-
Chakraborty R, Stivers DN, Zhong Y. 1996. Estimation of mutation rates from parentage exclusion data: applications to STR and VNTR loci. Mutat Res 354:41-48.
-
(1996)
Mutat Res
, vol.354
, pp. 41-48
-
-
Chakraborty, R.1
Stivers, D.N.2
Zhong, Y.3
-
12
-
-
0035892619
-
Non-fatherhood or mutation? A probabilistic approach to parental exclusion in paternity testing
-
Dawid AP, Mortera J, Pascali VL. 2001. Non-fatherhood or mutation? A probabilistic approach to parental exclusion in paternity testing. Forensic Sci Int 124:55-61.
-
(2001)
Forensic Sci Int
, vol.124
, pp. 55-61
-
-
Dawid, A.P.1
Mortera, J.2
Pascali, V.L.3
-
13
-
-
0029240186
-
Mutations in the sequence flanking the microsatellite at the KAP8 locus prevent the amplification of some alleles
-
Ede AJ, Crawford AM. 1995. Mutations in the sequence flanking the microsatellite at the KAP8 locus prevent the amplification of some alleles. Anim Genet 26:43-44.
-
(1995)
Anim Genet
, vol.26
, pp. 43-44
-
-
Ede, A.J.1
Crawford, A.M.2
-
14
-
-
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
-
15
-
-
0033010712
-
Size dependent mutation and microsatellite constraint
-
Falush D, Iwasa Y. 1999. Size dependent mutation and microsatellite constraint. Mol Biol Evol 16:960-966.
-
(1999)
Mol Biol Evol
, vol.16
, pp. 960-966
-
-
Falush, D.1
Iwasa, Y.2
-
16
-
-
0034488039
-
Genetic diversity of nine STRs in two northwest Iberian populations: Galicia and northern Portugal
-
Gusmao L, Sanchez-Diz P, Alves C, Lareu MV, Carracedo A, Amorim A. 2000. Genetic diversity of nine STRs in two northwest Iberian populations: Galicia and northern Portugal. Int J Legal Med 114:109-113.
-
(2000)
Int J Legal Med
, vol.114
, pp. 109-113
-
-
Gusmao, L.1
Sanchez-Diz, P.2
Alves, C.3
Lareu, M.V.4
Carracedo, A.5
Amorim, A.6
-
17
-
-
0034840316
-
Microdeletion in the FMR-1 gene: An apparent null allele using routine clinical PCR amplification
-
Hegde MR, Chong B, Fawkner M, Lambiris N, Peters H, Kenneson A, Warren ST, Love DR, McGaughran J. 2001. Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification. J Med Genet 38:624-629.
-
(2001)
J Med Genet
, vol.38
, pp. 624-629
-
-
Hegde, M.R.1
Chong, B.2
Fawkner, M.3
Lambiris, N.4
Peters, H.5
Kenneson, A.6
Warren, S.T.7
Love, D.R.8
McGaughran, J.9
-
18
-
-
0031736552
-
Sex biases in the mutation rate
-
Hurst LD, Ellegren H. 1998. Sex biases in the mutation rate. Trends Genet 14:446-452.
-
(1998)
Trends Genet
, vol.14
, pp. 446-452
-
-
Hurst, L.D.1
Ellegren, H.2
-
19
-
-
0029257180
-
Population structure, stepwise mutations, heterozygote deficiency and their implications in DNA forensics
-
Jin L, Chakraborty R. 1995. Population structure, stepwise mutations, heterozygote deficiency and their implications in DNA forensics. Heredity 74:274-285.
-
(1995)
Heredity
, vol.74
, pp. 274-285
-
-
Jin, L.1
Chakraborty, R.2
-
20
-
-
0030478158
-
Mutation rate varies among alleles at a microsatellite locus: Phylogenetic evidence
-
Jin L, Macaubas C, Hallmayer J, Kimura A, Mignot E. 1996. Mutation rate varies among alleles at a microsatellite locus: phylogenetic evidence. PNAS USA 93:15285-15288.
-
(1996)
PNAS USA
, vol.93
, pp. 15285-15288
-
-
Jin, L.1
Macaubas, C.2
Hallmayer, J.3
Kimura, A.4
Mignot, E.5
-
21
-
-
0347231556
-
Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs
-
Kayser M, Roewer L, Hedman M, Henke L, Henke J, Brauer S, Kruger C, Krawczak M, Nagy M, Dobosz T, Szibor R, de Knijff P, Stoneking M, Sajantila A. 2000. Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs. Am J Hum Genet 66:1580-1588.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1580-1588
-
-
Kayser, M.1
Roewer, L.2
Hedman, M.3
Henke, L.4
Henke, J.5
Brauer, S.6
Kruger, C.7
Krawczak, M.8
Nagy, M.9
Dobosz, T.10
Szibor, R.11
De Knijff, P.12
Stoneking, M.13
Sajantila, A.14
-
22
-
-
0034786938
-
Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090
-
Mertens G, Mommers N, Boutrand L, Gielis M, Vandenberghe A. 2001. Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090. Int J Legal Med 115:40-44.
-
(2001)
Int J Legal Med
, vol.115
, pp. 40-44
-
-
Mertens, G.1
Mommers, N.2
Boutrand, L.3
Gielis, M.4
Vandenberghe, A.5
-
23
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human cells
-
Miller SA, Dykes DD, Poleski HE 1988. A simple salting out procedure for extracting DNA from human cells. Nucleic Acids Res 16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Poleski, H.E.3
-
24
-
-
0015765702
-
A model of mutation appropriate to estimate the number of electrophoretically detectable alleles in a finite population
-
Ota T, Kimura M. 1973. A model of mutation appropriate to estimate the number of electrophoretically detectable alleles in a finite population. Genet Res 22:201-204.
-
(1973)
Genet Res
, vol.22
, pp. 201-204
-
-
Ota, T.1
Kimura, M.2
-
25
-
-
0026024236
-
DNA bioprints: Simple nonisotopic DNA fingerprints with biotinylated probes
-
Pena SDJ, Macedo AM, Gontijo NF, Medeiros AM, Ribeiro JC. 1991. DNA bioprints: simple nonisotopic DNA fingerprints with biotinylated probes. Electrophoresis 12:146-152.
-
(1991)
Electrophoresis
, vol.12
, pp. 146-152
-
-
Pena, S.D.J.1
Macedo, A.M.2
Gontijo, N.F.3
Medeiros, A.M.4
Ribeiro, J.C.5
-
26
-
-
0028879026
-
DNA diagnosis of human genetic individuality
-
Pena SD, Prado VF, Epplen JT 1995. DNA diagnosis of human genetic individuality. J Mol Med 73:555-564.
-
(1995)
J Mol Med
, vol.73
, pp. 555-564
-
-
Pena, S.D.1
Prado, V.F.2
Epplen, J.T.3
-
27
-
-
0000952520
-
Single-tube single-color multiplex PCR amplification of 10 polymorphic microsatellites (ALF10): A new powerful tool for DNA profiling
-
Pena SDJ. 1999. Single-tube single-color multiplex PCR amplification of 10 polymorphic microsatellites (ALF10): a new powerful tool for DNA profiling. Pure Appl Chem 71:1683-1690.
-
(1999)
Pure Appl Chem
, vol.71
, pp. 1683-1690
-
-
Pena, S.D.J.1
-
29
-
-
0012453776
-
-
Allelic frequency distribution of three STR loci (D12S1090 D3S1744, D18S849) in Argentina
-
Raimond E, Toscanini U, Haas E. 1998. Allelic frequency distribution of three STR loci (D12S1090, D3S1744, D18S849) in Argentina. Second European symposium on human identification. (Poster abstract: www.promega.com/geneticidproc/eusymp2proc/ab37.pdf).
-
(1998)
Second European Symposium on Human Identification
-
-
Raimond, E.1
Toscanini, U.2
Haas, E.3
-
30
-
-
0033614763
-
Microsatellite and trinucleotide repeat evolution: Evidence for mutational bias and different rates of evolution in different lineages
-
Rubinsztein DC, Amos W, Cooper G. 1999. Microsatellite and trinucleotide repeat evolution: evidence for mutational bias and different rates of evolution in different lineages. Phil Trans R Soc London B 354:1095-1099.
-
(1999)
Phil Trans R Soc London B
, vol.354
, pp. 1095-1099
-
-
Rubinsztein, D.C.1
Amos, W.2
Cooper, G.3
-
31
-
-
0032986618
-
Experimentally observed germline mutations at human micro- and minisatellite loci
-
Sajantila A, Lukka M, Syvanen AC. 1999. Experimentally observed germline mutations at human micro- and minisatellite loci. Eur J Hum Genet 7:263-266.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 263-266
-
-
Sajantila, A.1
Lukka, M.2
Syvanen, A.C.3
-
32
-
-
0030063477
-
Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19
-
Santos FR, Gerelsaikhan T, Munkhtuja B, Oyunsuren T, Epplen JT, Pena SD. 1996. Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19. Hum Genet 97:309-313.
-
(1996)
Hum Genet
, vol.97
, pp. 309-313
-
-
Santos, F.R.1
Gerelsaikhan, T.2
Munkhtuja, B.3
Oyunsuren, T.4
Epplen, J.T.5
Pena, S.D.6
-
33
-
-
0033808899
-
Evolutionary dynamics of microsatellite DNA
-
Schlötterer C. 2000. Evolutionary dynamics of microsatellite DNA. Chromosoma 109:365-371.
-
(2000)
Chromosoma
, vol.109
, pp. 365-371
-
-
Schlötterer, C.1
-
34
-
-
0034639682
-
Microsatellite instability in tumors as a model to study the process of microsatellite mutations
-
Sturzeneker R, Bevilacqua RAU, Haddad LA, Simpson AJG, Pena SDJ. 2000. Microsatellite instability in tumors as a model to study the process of microsatellite mutations. Hum Mol Genet 9:347-352.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 347-352
-
-
Sturzeneker, R.1
Bevilacqua, R.A.U.2
Haddad, L.A.3
Simpson, A.J.G.4
Pena, S.D.J.5
-
35
-
-
0029051470
-
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells
-
Talbot CC Jr, Avramopoulos D, Gerken S, Chakravarti A, Armour JA, Matsunami N, White R, Antonarakis SE. 1995. The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells. Hum Mol Genet 4:1193-1199.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1193-1199
-
-
Talbot C.C., Jr.1
Avramopoulos, D.2
Gerken, S.3
Chakravarti, A.4
Armour, J.A.5
Matsunami, N.6
White, R.7
Antonarakis, S.E.8
-
36
-
-
0024387394
-
Hypervariability of simple sequences as a general source for polymorphic DNA markers
-
Tautz D. 1989. Hypervariability of simple sequences as a general source for polymorphic DNA markers. Nucleic Acids Res 17:6463-6471.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 6463-6471
-
-
Tautz, D.1
-
37
-
-
0035864261
-
Sequenced allelic ladders and population genetics of a new STR multiplex system
-
Watson S, Allsop R, Foreman L, Kelsey Z, Gill P. 2001. Sequenced allelic ladders and population genetics of a new STR multiplex system. Forensic Sci Int 115: 207-217.
-
(2001)
Forensic Sci Int
, vol.115
, pp. 207-217
-
-
Watson, S.1
Allsop, R.2
Foreman, L.3
Kelsey, Z.4
Gill, P.5
-
38
-
-
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
|