{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,25]],"date-time":"2026-01-25T08:28:13Z","timestamp":1769329693233,"version":"3.49.0"},"reference-count":23,"publisher":"Springer Science and Business Media LLC","issue":"6","license":[{"start":{"date-parts":[[2012,9,1]],"date-time":"2012-09-01T00:00:00Z","timestamp":1346457600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Int J Legal Med"],"published-print":{"date-parts":[[2012,11]]},"DOI":"10.1007\/s00414-012-0768-5","type":"journal-article","created":{"date-parts":[[2012,8,31]],"date-time":"2012-08-31T07:19:24Z","timestamp":1346397564000},"page":"917-921","source":"Crossref","is-referenced-by-count":36,"title":["Comparative evaluation of alternative batteries of genetic markers to complement autosomal STRs in kinship investigations: autosomal indels vs. X-chromosome STRs"],"prefix":"10.1007","volume":"126","author":[{"given":"Cl\u00e1udia","family":"Gomes","sequence":"first","affiliation":[]},{"given":"Marta","family":"Magalh\u00e3es","sequence":"additional","affiliation":[]},{"given":"C\u00edntia","family":"Alves","sequence":"additional","affiliation":[]},{"given":"Ant\u00f3nio","family":"Amorim","sequence":"additional","affiliation":[]},{"given":"N\u00e1dia","family":"Pinto","sequence":"additional","affiliation":[]},{"given":"Leonor","family":"Gusm\u00e3o","sequence":"additional","affiliation":[]}],"member":"297","published-online":{"date-parts":[[2012,9,1]]},"reference":[{"key":"768_CR1","doi-asserted-by":"crossref","unstructured":"Pinto N, Magalh\u00e3es M, Conde-Sousa E, Gomes C, Pereira R, Alves C, Gusm\u00e3o L, Amorim A (2012) Assessing paternities with inconclusive STR results: the suitability of bi-allelic markers. Forensic Sci Int Genet. doi: 10.1016\/j.fsigen.2012.05.002","DOI":"10.1016\/j.fsigen.2012.05.002"},{"key":"768_CR2","doi-asserted-by":"crossref","first-page":"198","DOI":"10.1016\/j.fsigen.2008.02.002","volume":"2","author":"C Phillips","year":"2008","unstructured":"Phillips C, Fondevila M, Garc\u00eda-Magari\u00f1os M, Rodriguez A, Salas A, Carracedo A, Lareu MV (2008) Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic Sci Int Genet 2:198\u2013204. doi: 10.1016\/j.fsigen.2008.02.002","journal-title":"Forensic Sci Int Genet"},{"key":"768_CR3","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1016\/j.fsigss.2009.09.005","volume":"2","author":"R Pereira","year":"2009","unstructured":"Pereira R, Phillips C, Alves C, Amorim A, Carracedo \u00c1, Gusm\u00e3o L (2009) Insertion\/deletion polymorphisms: a multiplex assay and forensic applications. Forensic Sci Int Genet Suppl Ser 2:513\u2013515. doi: 10.1016\/j.fsigss.2009.09.005","journal-title":"Forensic Sci Int Genet Suppl Ser"},{"key":"768_CR4","doi-asserted-by":"crossref","first-page":"236","DOI":"10.1016\/j.fsigen.2010.02.007","volume":"5","author":"C B\u00f8rsting","year":"2011","unstructured":"B\u00f8rsting C, Morling N (2011) Mutations and\/or close relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers. Forensic Sci Int Genet 5:236\u2013241. doi: 10.1016\/j.fsigen.2010.02.007","journal-title":"Forensic Sci Int Genet"},{"key":"768_CR5","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1093\/genetics\/156.1.297","volume":"156","author":"MW Nachman","year":"2000","unstructured":"Nachman MW, Crowell SL (2000) Estimate of the mutation rate per nucleotide in humans. Genetics 156:297\u2013304","journal-title":"Genetics"},{"key":"768_CR6","doi-asserted-by":"crossref","unstructured":"Li L, Ge J, Zhang S, Guo J, Zhao S, Li C, Tang H, Davis C, Budowle B, Hou Y, Liu Y (2012) Maternity exclusion with a very high autosomal STRs kinship index. Int J Legal Med. doi: 10.1007\/s00414-012-0668-8","DOI":"10.1007\/s00414-012-0668-8"},{"key":"768_CR7","doi-asserted-by":"crossref","first-page":"496","DOI":"10.1016\/j.fsigss.2007.10.080","volume":"1","author":"C Bobillo","year":"2008","unstructured":"Bobillo C, Marino M, Sala A, Gusm\u00e3o L, Corach D (2008) X-STRs: relevance in complex kinship cases. Forensic Sci Int Genet Suppl Ser 1:496\u2013498. doi: 10.1016\/j.fsigss.2007.10.080","journal-title":"Forensic Sci Int Genet Suppl Ser"},{"key":"768_CR8","first-page":"53","volume":"73","author":"W Branicki","year":"2008","unstructured":"Branicki W, Wola\u0144ska-Nowak P, Parys-Proszek A (2008) Application of the Mentype Argus X-8 kit to forensic casework. Probl Forensic Sci 73:53\u201364","journal-title":"Probl Forensic Sci"},{"key":"768_CR9","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1016\/j.fsigss.2011.08.081","volume":"3","author":"C Gomes","year":"2011","unstructured":"Gomes C, Magalh\u00e3es M, Amorim A, Alves C, Pinto N, Gusm\u00e3o L (2011) How useful is your X in discerning pedigrees? Forensic Sci Int Genet Suppl Ser 3:161\u2013162. doi: 10.1016\/j.fsigss.2011.08.081","journal-title":"Forensic Sci Int Genet Suppl Ser"},{"key":"768_CR10","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/j.fsigen.2010.01.011","volume":"5","author":"N Pinto","year":"2010","unstructured":"Pinto N, Gusm\u00e3o L, Amorim A (2010) X-chromosome markers in kinship testing: a generalisation of the IBD approach identifying situations where their contribution is crucial. Forensic Sci Int Genet 5:27\u201332. doi: 10.1016\/j.fsigen.2010.01.011","journal-title":"Forensic Sci Int Genet"},{"key":"768_CR11","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1007\/s00414-002-0352-5","volume":"117","author":"R Szibor","year":"2003","unstructured":"Szibor R, Krawczak M, Hering S, Edelmann J, Kuhlisch E, Krause D (2003) Use of X-linked markers for forensic purposes. Int J Legal Med 117:67\u201374. doi: 10.1007\/s00414-002-0352-5","journal-title":"Int J Legal Med"},{"key":"768_CR12","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1016\/j.fsigen.2007.03.003","volume":"1","author":"R Szibor","year":"2007","unstructured":"Szibor R (2007) X-chromosomal markers: past, present and future. Forensic Sci Int Genet 1:93\u201399. doi: 10.1016\/j.fsigen.2007.03.003","journal-title":"Forensic Sci Int Genet"},{"key":"768_CR13","doi-asserted-by":"crossref","first-page":"3682","DOI":"10.1002\/elps.200900274","volume":"30","author":"R Pereira","year":"2009","unstructured":"Pereira R, Phillips C, Alves C, Amorim A, Carracedo \u00c1, Gusm\u00e3o L (2009) A new multiplex for human identification using insertion\/deletion polymorphisms. Electrophoresis 30:3682\u20133690. doi: 10.1002\/elps.200900274","journal-title":"Electrophoresis"},{"key":"768_CR14","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1016\/S0379-0738(00)00147-X","volume":"110","author":"T Egeland","year":"2000","unstructured":"Egeland T, Mostad P, Mev\u00e5g B, Stenersen M (2000) Beyond traditional paternity and identification cases. Selecting the most probable pedigree. Forensic Sci Int 110:47\u201359. doi: 10.1016\/S0379-0738(00)00147-X","journal-title":"Forensic Sci Int"},{"key":"768_CR15","first-page":"364","volume":"11","author":"A Amorim","year":"2006","unstructured":"Amorim A, Alves C, Gusm\u00e3o L, Pereira L (2006) Extended Northern Portuguese database on 21 autosomal STRs used in genetic identification. Prog Forensic Genet 11:364\u2013366. doi: 10.1016\/j.ics.2005.09.026","journal-title":"Prog Forensic Genet"},{"key":"768_CR16","unstructured":"American Association of Blood Banks (AABB) (2008) Annual report summary for testing in 2008. Available at http:\/\/www.aabb.org\/sa\/facilities\/Documents\/ rtannrpt08.pdf. Accessed in January 26, 2011"},{"key":"768_CR17","doi-asserted-by":"crossref","unstructured":"Jobling MA, Hurles M, Tyler-Smith C (2004) Human evolutionary genetics: origins, peoples & disease. Garland Sci. doi: 10.1007\/s00439-004-1138-2","DOI":"10.1007\/s00439-004-1138-2"},{"key":"768_CR18","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1007\/s004140100215","volume":"115","author":"C Alves","year":"2001","unstructured":"Alves C, Amorim A, Gusm\u00e3o L, Pereira L (2001) VWA STR genotyping: further inconsistencies between Perkin-Elmer and Promega kits. Int J Legal Med 115:97\u201399. doi: 10.1007\/s004140100215","journal-title":"Int J Legal Med"},{"key":"768_CR19","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1016\/S0379-0738(00)00182-1","volume":"112","author":"A Cotton","year":"2000","unstructured":"Cotton A, Allsop RF, Guest L, Frazier R, Koumi P, Callow P, Seager A, Sparkes RL (2000) Validation of the AMPFlSTR SGM plus system for use in forensic casework. Forensic Sci Int 112:151\u2013161. doi: 10.1016\/S0379-0738(00)00182-1","journal-title":"Forensic Sci Int"},{"key":"768_CR20","doi-asserted-by":"crossref","first-page":"220","DOI":"10.1016\/S0379-0738(03)00035-5","volume":"133","author":"C Leibelt","year":"2003","unstructured":"Leibelt C, Budowle B, Collins P, Daoudi Y, Moretti T, Nunn G, Reeder D, Roby R (2003) Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles. Forensic Sci Int 133:220\u2013227. doi: 10.1016\/S0379-0738(03)00035-5","journal-title":"Forensic Sci Int"},{"key":"768_CR21","doi-asserted-by":"crossref","unstructured":"Edelmann J, Lutz-Bonengel S, Naue J, Hering S (2011) X-chromosomal haplotype frequencies of four linkage groups using the Investigator Argus X-12 Kit. Forensic Sci Int Genet. doi: 10.1016\/j.fsigen.2011.01.001","DOI":"10.1016\/j.fsigen.2011.01.001"},{"key":"768_CR22","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1016\/j.fsigss.2011.08.004","volume":"3","author":"M Magalh\u00e3es","year":"2011","unstructured":"Magalh\u00e3es M, Pinto N, Gomes C, Amorim A, Alves C, Gusm\u00e3o L (2011) When the alleged father is a close relative of the real father: the utility of insertion\/deletion polymorphisms. Forensic Sci Int Genet Suppl Ser 3:9\u201310. doi: 10.1016\/j.fsigss.2011.08.004","journal-title":"Forensic Sci Int Genet Suppl Ser"},{"key":"768_CR23","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1007\/s00414-009-0413-0","volume":"124","author":"M Nothnagel","year":"2010","unstructured":"Nothnagel M, Schmidtke J, Krawczak M (2010) Potentials and limits of pairwise kinship analysis using autosomal short tandem repeat loci. Int J Legal Med 124:205\u2013215. doi: 10.1007\/s00414-009-0413-0","journal-title":"Int J Legal Med"}],"container-title":["International Journal of Legal Medicine"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00414-012-0768-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00414-012-0768-5\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00414-012-0768-5","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,1,28]],"date-time":"2022-01-28T00:09:43Z","timestamp":1643328583000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00414-012-0768-5"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,9,1]]},"references-count":23,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2012,11]]}},"alternative-id":["768"],"URL":"https:\/\/doi.org\/10.1007\/s00414-012-0768-5","relation":{},"ISSN":["0937-9827","1437-1596"],"issn-type":[{"value":"0937-9827","type":"print"},{"value":"1437-1596","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,9,1]]}}}