-
1
-
-
0031727378
-
The Xg blood group system: a review
-
Tippett P., and Ellis N.A. The Xg blood group system: a review. Transfus. Med. Rev. 12 4 (1998) 233-257
-
(1998)
Transfus. Med. Rev.
, vol.12
, Issue.4
, pp. 233-257
-
-
Tippett, P.1
Ellis, N.A.2
-
2
-
-
0026044146
-
Tetranucleotide repeat polymorphism at the HPRT locus
-
Hearne C.M., and Todd J.A. Tetranucleotide repeat polymorphism at the HPRT locus. Nucleic Acids Res. 19 19 (1991) 5450
-
(1991)
Nucleic Acids Res.
, vol.19
, Issue.19
, pp. 5450
-
-
Hearne, C.M.1
Todd, J.A.2
-
3
-
-
0026551039
-
Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups
-
Edwards A., Hammond H.A., Jin L., Caskey C.T., and Chakraborty R. Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. Genomics 12 2 (1992) 241-253
-
(1992)
Genomics
, vol.12
, Issue.2
, pp. 241-253
-
-
Edwards, A.1
Hammond, H.A.2
Jin, L.3
Caskey, C.T.4
Chakraborty, R.5
-
4
-
-
0031679152
-
Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA)
-
Desmarais D., Zhong Y., Chakraborty R., Perreault C., and Busque L. Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA). J. Forensic Sci. 43 5 (1998) 1046-1049
-
(1998)
J. Forensic Sci.
, vol.43
, Issue.5
, pp. 1046-1049
-
-
Desmarais, D.1
Zhong, Y.2
Chakraborty, R.3
Perreault, C.4
Busque, L.5
-
5
-
-
0031005894
-
Duplex PCR of the Y-27H39 and HPRT loci with reference to Japanese population data on the HPRT locus
-
Kishida T., Wang W., Fukuda M., and Tamaki Y. Duplex PCR of the Y-27H39 and HPRT loci with reference to Japanese population data on the HPRT locus. Nippon Hoigaku Zasshi 51 2 (1997) 67-69
-
(1997)
Nippon Hoigaku Zasshi
, vol.51
, Issue.2
, pp. 67-69
-
-
Kishida, T.1
Wang, W.2
Fukuda, M.3
Tamaki, Y.4
-
6
-
-
0014378082
-
On the utilization of erythrocyte acid phosphatase polymorphism in paternity evaluation
-
Krüger J., Fuhrmann W., Lichte K.H., and Steffens C. On the utilization of erythrocyte acid phosphatase polymorphism in paternity evaluation. Dtsch. Z. Gesamte Gerichtl. Med. 64 2 (1968) 127-146
-
(1968)
Dtsch. Z. Gesamte Gerichtl. Med.
, vol.64
, Issue.2
, pp. 127-146
-
-
Krüger, J.1
Fuhrmann, W.2
Lichte, K.H.3
Steffens, C.4
-
7
-
-
0037501238
-
Use of X-linked markers for forensic purposes
-
Szibor R., Krawczak M., Hering S., Edelmann J., Kuhlisch E., and Krause D. Use of X-linked markers for forensic purposes. Int. J. Legal Med. 117 2 (2003) 67-74
-
(2003)
Int. J. Legal Med.
, vol.117
, Issue.2
, pp. 67-74
-
-
Szibor, R.1
Krawczak, M.2
Hering, S.3
Edelmann, J.4
Kuhlisch, E.5
Krause, D.6
-
8
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculus L.)
-
Lyon M.F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 190 (1961) 372-373
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.F.1
-
9
-
-
17144464108
-
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
-
Clement-Jones M., Schiller S., Rao E., Blaschke R.J., Zuniga A., Zeller R., Robson S.C., Binder G., Glass I., Strachan T., Lindsay S., and Rappold G.A. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Hum. Mol. Genet. 9 5 (2000) 695-702
-
(2000)
Hum. Mol. Genet.
, vol.9
, Issue.5
, pp. 695-702
-
-
Clement-Jones, M.1
Schiller, S.2
Rao, E.3
Blaschke, R.J.4
Zuniga, A.5
Zeller, R.6
Robson, S.C.7
Binder, G.8
Glass, I.9
Strachan, T.10
Lindsay, S.11
Rappold, G.A.12
-
11
-
-
0031752939
-
Pseudo-exclusion from paternity due to maternal uniparental disomy 16
-
Bein G., Driller B., Schurmann M., Schneider P.M., and Kirchner H. Pseudo-exclusion from paternity due to maternal uniparental disomy 16. Int. J. Legal Med. 111 6 (1998) 328-330
-
(1998)
Int. J. Legal Med.
, vol.111
, Issue.6
, pp. 328-330
-
-
Bein, G.1
Driller, B.2
Schurmann, M.3
Schneider, P.M.4
Kirchner, H.5
-
13
-
-
0037326103
-
Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study
-
Bojesen A., Juul S., and Gravholt C.H. Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J. Clin. Endocrinol. Metab. 88 2 (2003) 622-626
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, Issue.2
, pp. 622-626
-
-
Bojesen, A.1
Juul, S.2
Gravholt, C.H.3
-
14
-
-
8544258065
-
Evaluation of Y-chromosomal STRs: a multicenter study
-
141-129
-
Kayser M., Caglia A., Corach D., Fretwell N., Gehrig C., Graziosi G., Heidorn F., Herrmann S., Herzog B., Hidding M., Honda K., Jobling M., Krawczak M., Leim K., Meuser S., Meyer E., Oesterreich W., Pandya A., Parson W., Penacino G., Perez-Lezaun A., Piccinini A., Prinz M., Schmitt C., Roewer L., et al. Evaluation of Y-chromosomal STRs: a multicenter study. Int. J. Legal Med. 110 3 (1997) 125-133 141-129
-
(1997)
Int. J. Legal Med.
, vol.110
, Issue.3
, pp. 125-133
-
-
Kayser, M.1
Caglia, A.2
Corach, D.3
Fretwell, N.4
Gehrig, C.5
Graziosi, G.6
Heidorn, F.7
Herrmann, S.8
Herzog, B.9
Hidding, M.10
Honda, K.11
Jobling, M.12
Krawczak, M.13
Leim, K.14
Meuser, S.15
Meyer, E.16
Oesterreich, W.17
Pandya, A.18
Parson, W.19
Penacino, G.20
Perez-Lezaun, A.21
Piccinini, A.22
Prinz, M.23
Schmitt, C.24
Roewer, L.25
more..
-
15
-
-
0026651433
-
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts
-
Roewer L., Arnemann J., Spurr N.K., Grzeschik K.H., and Epplen J.T. Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts. Hum. Genet. 89 4 (1992) 389-394
-
(1992)
Hum. Genet.
, vol.89
, Issue.4
, pp. 389-394
-
-
Roewer, L.1
Arnemann, J.2
Spurr, N.K.3
Grzeschik, K.H.4
Epplen, J.T.5
-
16
-
-
0027462891
-
A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci
-
Mahtani M.M., and Willard H.F. A polymorphic X-linked tetranucleotide repeat locus displaying a high rate of new mutation: implications for mechanisms of mutation at short tandem repeat loci. Hum. Mol. Genet. 2 4 (1993) 431-437
-
(1993)
Hum. Mol. Genet.
, vol.2
, Issue.4
, pp. 431-437
-
-
Mahtani, M.M.1
Willard, H.F.2
-
17
-
-
18744379166
-
The HumARA genotype is linked to spinal and bulbar muscular dystrophy and some further disease risks and should no longer be used as a DNA marker for forensic purposes
-
Szibor R., Hering S., and Edelmann J. The HumARA genotype is linked to spinal and bulbar muscular dystrophy and some further disease risks and should no longer be used as a DNA marker for forensic purposes. Int. J. Legal Med. 119 3 (2005) 179-180
-
(2005)
Int. J. Legal Med.
, vol.119
, Issue.3
, pp. 179-180
-
-
Szibor, R.1
Hering, S.2
Edelmann, J.3
-
18
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada A.R., Wilson E.M., Lubahn D.B., Harding A.E., and Fischbeck K.H. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352 6330 (1991) 77-79
-
(1991)
Nature
, vol.352
, Issue.6330
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
19
-
-
11144291546
-
DXS10011: studies on structure, allele distribution in three populations and genetic linkage to further q-telomeric chromosome X markers
-
Hering S., Brundirs N., Kuhlisch E., Edelmann J., Plate I., Benecke M., Van P.H., Michael M., and Szibor R. DXS10011: studies on structure, allele distribution in three populations and genetic linkage to further q-telomeric chromosome X markers. Int. J. Legal Med. 118 6 (2004) 313-319
-
(2004)
Int. J. Legal Med.
, vol.118
, Issue.6
, pp. 313-319
-
-
Hering, S.1
Brundirs, N.2
Kuhlisch, E.3
Edelmann, J.4
Plate, I.5
Benecke, M.6
Van, P.H.7
Michael, M.8
Szibor, R.9
-
20
-
-
33645829610
-
MiniX-STR multiplex system population study in Japan and application to degraded DNA analysis
-
Asamura H., Sakai H., Kobayashi K., Ota M., and Fukushima H. MiniX-STR multiplex system population study in Japan and application to degraded DNA analysis. Int. J. Legal Med. (2006) 1-8
-
(2006)
Int. J. Legal Med.
, pp. 1-8
-
-
Asamura, H.1
Sakai, H.2
Kobayashi, K.3
Ota, M.4
Fukushima, H.5
-
21
-
-
4243082140
-
Prenatal exclusion without involving the putative fathers of an incestuous father-daughter parenthood
-
Schmidtke J., Kuhnau W., Wand D., Edelmann J., Szibor R., and Krawczak M. Prenatal exclusion without involving the putative fathers of an incestuous father-daughter parenthood. Prenat. Diagn. 24 8 (2004) 662-664
-
(2004)
Prenat. Diagn.
, vol.24
, Issue.8
, pp. 662-664
-
-
Schmidtke, J.1
Kuhnau, W.2
Wand, D.3
Edelmann, J.4
Szibor, R.5
Krawczak, M.6
-
22
-
-
34248564714
-
DXS10079, DXS10074 and DXS10075 are STRs located within a 280-kb region of Xq12 and provide stable haplotypes useful for complex kinship cases
-
Hering S., Augustin C., Edelmann J., Heidel M., Dressler J., Rodig H., Kuhlisch E., and Szibor R. DXS10079, DXS10074 and DXS10075 are STRs located within a 280-kb region of Xq12 and provide stable haplotypes useful for complex kinship cases. Int. J. Legal Med. (2005) 1-9
-
(2005)
Int. J. Legal Med.
, pp. 1-9
-
-
Hering, S.1
Augustin, C.2
Edelmann, J.3
Heidel, M.4
Dressler, J.5
Rodig, H.6
Kuhlisch, E.7
Szibor, R.8
-
23
-
-
34248527793
-
-
H. Rodig, F. Kloep, L. Weißbach, C. Augustin, J. Edelmann, S. Hering, R. Szibor, F. Götz, W. Brabetz, Evaluation of 7 X-chromosomal Short Tandem Repeat loci located within the Xq26 region, in press.
-
-
-
-
24
-
-
0037127432
-
Validation of the STR DXS7424 and the linkage situation on the X-chromosome
-
Edelmann J., Hering S., Kuhlisch E., and Szibor R. Validation of the STR DXS7424 and the linkage situation on the X-chromosome. Forensic Sci. Int. 125 (2002) 217-222
-
(2002)
Forensic Sci. Int.
, vol.125
, pp. 217-222
-
-
Edelmann, J.1
Hering, S.2
Kuhlisch, E.3
Szibor, R.4
-
25
-
-
27744583288
-
Haplotyping of STR cluster DXS6801-DXS6809-DXS6789 on Xq21 provides a powerful tool for kinship testing
-
Szibor R., Hering S., Kuhlisch E., Plate I., Demberger S., Krawczak M., and Edelmann J. Haplotyping of STR cluster DXS6801-DXS6809-DXS6789 on Xq21 provides a powerful tool for kinship testing. Int. J. Legal Med. 119 6 (2005) 363-369
-
(2005)
Int. J. Legal Med.
, vol.119
, Issue.6
, pp. 363-369
-
-
Szibor, R.1
Hering, S.2
Kuhlisch, E.3
Plate, I.4
Demberger, S.5
Krawczak, M.6
Edelmann, J.7
-
26
-
-
34248506671
-
Forensic evaluation of three closely linked STR markers in a 13kb region at Xp11.23
-
Augustin C., Cichy R., Hering S., Edelmann J., Kuhlisch E., and Szibor R. Forensic evaluation of three closely linked STR markers in a 13kb region at Xp11.23. Int. Congress Ser. 1239 (2006) 311-314
-
(2006)
Int. Congress Ser.
, vol.1239
, pp. 311-314
-
-
Augustin, C.1
Cichy, R.2
Hering, S.3
Edelmann, J.4
Kuhlisch, E.5
Szibor, R.6
-
27
-
-
34248507070
-
Study of six X-linked tetranucleotide microsatellites: population data from five Spanish regions
-
Zarrabeitia M.T., Alonso A., Martin J., Gonzalez-Gay M.A., Martin-Escudero J.C., de Pancorbo M.M., Sanz P., Ruiz-Cabello F., and Riancho J.A. Study of six X-linked tetranucleotide microsatellites: population data from five Spanish regions. Int. J. Legal Med. (2005) 1-4
-
(2005)
Int. J. Legal Med.
, pp. 1-4
-
-
Zarrabeitia, M.T.1
Alonso, A.2
Martin, J.3
Gonzalez-Gay, M.A.4
Martin-Escudero, J.C.5
de Pancorbo, M.M.6
Sanz, P.7
Ruiz-Cabello, F.8
Riancho, J.A.9
-
28
-
-
8444236785
-
Genetic analysis of 18 X-linked short tandem repeat markers in Korean population
-
Shin S.H., Yu J.S., Park S.W., Min G.S., and Chung K.W. Genetic analysis of 18 X-linked short tandem repeat markers in Korean population. Forensic Sci. Int. 147 1 (2005) 35-41
-
(2005)
Forensic Sci. Int.
, vol.147
, Issue.1
, pp. 35-41
-
-
Shin, S.H.1
Yu, J.S.2
Park, S.W.3
Min, G.S.4
Chung, K.W.5
-
29
-
-
25144462722
-
Development of a pentaplex X-chromosomal short tandem repeat typing system and population genetic studies
-
Tabbada K.A., De Ungria M.C., Faustino L.P., Athanasiadou D., Stradmann-Bellinghausen B., and Schneider P.M. Development of a pentaplex X-chromosomal short tandem repeat typing system and population genetic studies. Forensic Sci. Int. 154 2/3 (2005) 173-180
-
(2005)
Forensic Sci. Int.
, vol.154
, Issue.2-3
, pp. 173-180
-
-
Tabbada, K.A.1
De Ungria, M.C.2
Faustino, L.P.3
Athanasiadou, D.4
Stradmann-Bellinghausen, B.5
Schneider, P.M.6
-
30
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich D.E., Cargill M., Bolk S., Ireland J., Sabeti P.C., Richter D.J., Lavery T., Kouyoumjian R., Farhadian S.F., Ward R., and Lander E.S. Linkage disequilibrium in the human genome. Nature 411 6834 (2001) 199-204
-
(2001)
Nature
, vol.411
, Issue.6834
, pp. 199-204
-
-
Reich, D.E.1
Cargill, M.2
Bolk, S.3
Ireland, J.4
Sabeti, P.C.5
Richter, D.J.6
Lavery, T.7
Kouyoumjian, R.8
Farhadian, S.F.9
Ward, R.10
Lander, E.S.11
-
31
-
-
0032006951
-
Using mitochondrial and nuclear DNA markers to reconstruct human evolution
-
Jorde L.B., Bamshad M., and Rogers A.R. Using mitochondrial and nuclear DNA markers to reconstruct human evolution. Bioessays 20 2 (1998) 126-136
-
(1998)
Bioessays
, vol.20
, Issue.2
, pp. 126-136
-
-
Jorde, L.B.1
Bamshad, M.2
Rogers, A.R.3
-
32
-
-
0036180886
-
Extensive linkage disequilibrium in small human populations in Eurasia
-
Kaessmann H., Zollner S., Gustafsson A.C., Wiebe V., Laan M., Lundeberg J., Uhlen M., and Paabo S. Extensive linkage disequilibrium in small human populations in Eurasia. Am. J. Hum. Genet. 70 3 (2002) 673-685
-
(2002)
Am. J. Hum. Genet.
, vol.70
, Issue.3
, pp. 673-685
-
-
Kaessmann, H.1
Zollner, S.2
Gustafsson, A.C.3
Wiebe, V.4
Laan, M.5
Lundeberg, J.6
Uhlen, M.7
Paabo, S.8
-
33
-
-
0032744180
-
Validation of the HumDXS6807 short tandem repeat polymorphism for forensic application
-
Edelmann J., and Szibor R. Validation of the HumDXS6807 short tandem repeat polymorphism for forensic application. Electrophoresis 20 14 (1999) 2844-2846
-
(1999)
Electrophoresis
, vol.20
, Issue.14
, pp. 2844-2846
-
-
Edelmann, J.1
Szibor, R.2
-
34
-
-
0035961031
-
16 X-chromosome STR loci frequency data from a German population
-
Edelmann J., Hering S., Michael M., Lessig R., Deichsel D., Meier-Sundhausen G., Roewer L., Plate I., and Szibor R. 16 X-chromosome STR loci frequency data from a German population. Forensic Sci. Int. 124 2/3 (2001) 215-218
-
(2001)
Forensic Sci. Int.
, vol.124
, Issue.2-3
, pp. 215-218
-
-
Edelmann, J.1
Hering, S.2
Michael, M.3
Lessig, R.4
Deichsel, D.5
Meier-Sundhausen, G.6
Roewer, L.7
Plate, I.8
Szibor, R.9
-
35
-
-
0033918693
-
Development of the X-linked tetrameric microsatellite marker DXS9898 for forensic purposes
-
Hering S., and Szibor R. Development of the X-linked tetrameric microsatellite marker DXS9898 for forensic purposes. J. Forensic Sci. 45 4 (2000) 929-931
-
(2000)
J. Forensic Sci.
, vol.45
, Issue.4
, pp. 929-931
-
-
Hering, S.1
Szibor, R.2
-
36
-
-
11444258603
-
Validation of the X-linked STR DXS6801
-
Edelmann J., and Szibor R. Validation of the X-linked STR DXS6801. Forensic Sci. Int. 148 (2005) 219-220
-
(2005)
Forensic Sci. Int.
, vol.148
, pp. 219-220
-
-
Edelmann, J.1
Szibor, R.2
-
37
-
-
0042430139
-
Validation of the X-chromosomal STR DXS6809
-
Edelmann J., Deichsel D., Plate I., Kaser M., and Szibor R. Validation of the X-chromosomal STR DXS6809. Int. J. Legal Med. 117 4 (2003) 241-244
-
(2003)
Int. J. Legal Med.
, vol.117
, Issue.4
, pp. 241-244
-
-
Edelmann, J.1
Deichsel, D.2
Plate, I.3
Kaser, M.4
Szibor, R.5
-
38
-
-
0035371810
-
Development of the X-linked tetrameric microsatellite marker HumDXS6789 for forensic purposes
-
Hering S., Kuhlisch E., and Szibor R. Development of the X-linked tetrameric microsatellite marker HumDXS6789 for forensic purposes. Forensic Sci. Int. 119 1 (2001) 42-46
-
(2001)
Forensic Sci. Int.
, vol.119
, Issue.1
, pp. 42-46
-
-
Hering, S.1
Kuhlisch, E.2
Szibor, R.3
-
39
-
-
0035063674
-
DXS101: a highly polymorphic X-linked STR
-
Edelmann J., and Szibor R. DXS101: a highly polymorphic X-linked STR. Int. J. Legal Med. 114 4/5 (2001) 301-304
-
(2001)
Int. J. Legal Med.
, vol.114
, Issue.4-5
, pp. 301-304
-
-
Edelmann, J.1
Szibor, R.2
-
40
-
-
32944460951
-
DXS6797 contains two STRs which can be easily haplotyped in both sexes
-
Poetsch M., Repenning A., Lignitz E., Kuhlisch E., and Szibor R. DXS6797 contains two STRs which can be easily haplotyped in both sexes. Int. J. Legal Med. 120 2 (2006) 61-66
-
(2006)
Int. J. Legal Med.
, vol.120
, Issue.2
, pp. 61-66
-
-
Poetsch, M.1
Repenning, A.2
Lignitz, E.3
Kuhlisch, E.4
Szibor, R.5
-
41
-
-
26444537975
-
Development of two pentaplex systems with X-chromosomal STR loci and their allele frequencies in a northeast German population
-
Poetsch M., Petersmann H., Repenning A., and Lignitz E. Development of two pentaplex systems with X-chromosomal STR loci and their allele frequencies in a northeast German population. Forensic Sci. Int. 155 1 (2005) 71-76
-
(2005)
Forensic Sci. Int.
, vol.155
, Issue.1
, pp. 71-76
-
-
Poetsch, M.1
Petersmann, H.2
Repenning, A.3
Lignitz, E.4
-
42
-
-
33645915134
-
Forensic validation of the X-chromosomal STR-markers GATA165B12, GATA164A09, DXS9908 and DXS7127 in German population
-
Edelmann J., Lessig R., Willenberg A., Wildgrube R., Hering S., and Szibor R. Forensic validation of the X-chromosomal STR-markers GATA165B12, GATA164A09, DXS9908 and DXS7127 in German population. Int. Congress Ser. 1239 (2006) 298-300
-
(2006)
Int. Congress Ser.
, vol.1239
, pp. 298-300
-
-
Edelmann, J.1
Lessig, R.2
Willenberg, A.3
Wildgrube, R.4
Hering, S.5
Szibor, R.6
-
43
-
-
0038691576
-
Sequence structure and population data of the X-linked markers DXS7423 and DXS8377-clarification of conflicting statements published by two working groups
-
Szibor R., Edelmann J., Zarrabeitia M.T., and Riancho J.A. Sequence structure and population data of the X-linked markers DXS7423 and DXS8377-clarification of conflicting statements published by two working groups. Forensic Sci. Int. 134 1 (2003) 72-73
-
(2003)
Forensic Sci. Int.
, vol.134
, Issue.1
, pp. 72-73
-
-
Szibor, R.1
Edelmann, J.2
Zarrabeitia, M.T.3
Riancho, J.A.4
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