-
2
-
-
0034783457
-
VWA STR genotyping: Further inconsistencies between Perkin-Elmer and Promega kits
-
Alves C., Amorim A., Gusmao L., Pereira L. VWA STR genotyping: further inconsistencies between Perkin-Elmer and Promega kits. Int. J. Leg. Med. 115:2001;97-99
-
(2001)
Int. J. Leg. Med.
, vol.115
, pp. 97-99
-
-
Alves, C.1
Amorim, A.2
Gusmao, L.3
Pereira, L.4
-
4
-
-
0034792605
-
Non-amplification of an allele of the D8S1179 locus due to a point mutation
-
Han G.R., Song E.S., Hwang J.J. Non-amplification of an allele of the D8S1179 locus due to a point mutation. Int. J. Leg. Med. 115:2001;45-47
-
(2001)
Int. J. Leg. Med.
, vol.115
, pp. 45-47
-
-
Han, G.R.1
Song, E.S.2
Hwang, J.J.3
-
5
-
-
85014292939
-
Multiplex STR genotyping: Comparison study, population data and new sequence information
-
B. Brinkman, A. Carracedo (Eds.), Excerpta Medica, Elsevier, Amsterdam
-
C. Alves, L. Gusmao, L. Pereira, A. Amorim, Multiplex STR genotyping: comparison study, population data and new sequence information, in: B. Brinkman, A. Carracedo (Eds.), Progress in Forensic Genetics, vol. 9, Excerpta Medica, Elsevier, Amsterdam, 2003, pp. 131-135.
-
(2003)
Progress in Forensic Genetics
, vol.9
, pp. 131-135
-
-
Alves, C.1
Gusmao, L.2
Pereira, L.3
Amorim, A.4
-
6
-
-
0037764728
-
Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles
-
Leibelt C., Budowle B., Collins P., Daoudi Y., Moretti T., Nunn G., Reeder D., Roby R. Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles. Forensic Sci. Int. 133:2003;220-227
-
(2003)
Forensic Sci. Int.
, vol.133
, pp. 220-227
-
-
Leibelt, C.1
Budowle, B.2
Collins, P.3
Daoudi, Y.4
Moretti, T.5
Nunn, G.6
Reeder, D.7
Roby, R.8
-
7
-
-
0030462847
-
The validation of a 7-locus multiplex STR test for use in forensic casework. I. Mixtures, ageing, degradation and species studies
-
Sparkes R., Kimpton C., Watson S., Oldroyd N., Clayton T., Barnett L., Arnold J., Thomson C., Hale R., Chapman J., Urquhart A., Gill P. The validation of a 7-locus multiplex STR test for use in forensic casework. I. Mixtures, ageing, degradation and species studies. Int. J. Leg. Med. 109:1996;186-194
-
(1996)
Int. J. Leg. Med.
, vol.109
, pp. 186-194
-
-
Sparkes, R.1
Kimpton, C.2
Watson, S.3
Oldroyd, N.4
Clayton, T.5
Barnett, L.6
Arnold, J.7
Thomson, C.8
Hale, R.9
Chapman, J.10
Urquhart, A.11
Gill, P.12
-
8
-
-
0033812929
-
A rare mutation in the amelogenin gene and its potential investigative ramifications
-
Roffey P.E., Eckhoff C.I., Kuhl J.L. A rare mutation in the amelogenin gene and its potential investigative ramifications. J. Forensic Sci. 45:2000;1016-1019
-
(2000)
J. Forensic Sci.
, vol.45
, pp. 1016-1019
-
-
Roffey, P.E.1
Eckhoff, C.I.2
Kuhl, J.L.3
-
9
-
-
0031682687
-
Commentary on M.C. Kline, B. Jenkins, S. Rodgers: Non-amplification of a vWA allele
-
Walsh S. Commentary on M.C. Kline, B. Jenkins, S. Rodgers: non-amplification of a vWA allele. J. Forensic Sci. 43:1998;1103-1104
-
(1998)
J. Forensic Sci.
, vol.43
, pp. 1103-1104
-
-
Walsh, S.1
-
10
-
-
17744397106
-
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: Novel truncating mutations in the FGA and FGG genes
-
Neerman-Arbez M., de Moerloose P., Honsberger A., Parlier G., Arnuti B., Biron C., Borg J.Y., Eber S., Meili E., Peter-Salonen K., Ripoll L., Vervel C., d'Oiron R., Staeger P., Antonarakis S.E., Morris M.A. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. Hum. Genet. 108:2001;237-240
-
(2001)
Hum. Genet.
, vol.108
, pp. 237-240
-
-
Neerman-Arbez, M.1
De Moerloose, P.2
Honsberger, A.3
Parlier, G.4
Arnuti, B.5
Biron, C.6
Borg, J.Y.7
Eber, S.8
Meili, E.9
Peter-Salonen, K.10
Ripoll, L.11
Vervel, C.12
D'Oiron, R.13
Staeger, P.14
Antonarakis, S.E.15
Morris, M.A.16
-
11
-
-
2142751535
-
Two novel fibrinogen variants found in patients with pulmonary embolism and their families
-
Hanss M.M.L., Ffrench P.O., Mornex J.F., Chabuet M., Biot F., De Mazancourt P., Dechavanne M. Two novel fibrinogen variants found in patients with pulmonary embolism and their families. J. Thromb. Haemost. 1:2003;1251-1257
-
(2003)
J. Thromb. Haemost.
, vol.1
, pp. 1251-1257
-
-
Hanss, M.M.L.1
Ffrench, P.O.2
Mornex, J.F.3
Chabuet, M.4
Biot, F.5
De Mazancourt, P.6
Dechavanne, M.7
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