312 related articles for article (PubMed ID: 14979352)
1. Mutation in the STR locus D21S1 1 of father causing allele mismatch in the child.
Thangaraj K; Reddy AG; Singh L
J Forensic Sci; 2004 Jan; 49(1):99-103. PubMed ID: 14979352
[TBL] [Abstract][Full Text] [Related]
2. Single and double incompatibility at vWA and D8S1179/D21S11 loci between mother and child: implications in kinship analysis.
Narkuti V; Vellanki RN; Anubrolu N; Doddapaneni KK; Gandhi Kaza PC; Mangamoori LN
Clin Chim Acta; 2008 Sep; 395(1-2):162-5. PubMed ID: 18503761
[TBL] [Abstract][Full Text] [Related]
3. Analysis of a paternity case in which the alleged father was deceased: single locus mismatch.
Tsuji A; Ishiko A; Inoue H; Kudo K; Ikeda N
Fukuoka Igaku Zasshi; 2005 Mar; 96(3):76-80. PubMed ID: 15920965
[TBL] [Abstract][Full Text] [Related]
4. Microsatellite mutation in the maternally/paternally transmitted D18S51 locus: two cases of allele mismatch in the child.
Narkuti V; Vellanki RN; Gandhi KP; Doddapaneni KK; Yelavarthi PD; Mangamoori LN
Clin Chim Acta; 2007 Jun; 381(2):171-5. PubMed ID: 17428456
[TBL] [Abstract][Full Text] [Related]
5. Combining autosomal and Y-chromosomal short tandem repeat data in paternity testing with male child: methods and application.
Ayadi I; Mahfoudh-Lahiani N; Makni H; Ammar-Keskes L; Rebaï A
J Forensic Sci; 2007 Sep; 52(5):1068-72. PubMed ID: 17645485
[TBL] [Abstract][Full Text] [Related]
6. Mother-child double incompatibility at vWA and D5S818 loci in paternity testing.
Narkuti V; Vellanki RN; Gandhi KP; Mangamoori LN
Clin Chem Lab Med; 2007; 45(10):1288-91. PubMed ID: 17727308
[TBL] [Abstract][Full Text] [Related]
7. Paternity analysis in special fatherless cases without direct testing of alleged father.
Mixich F; Ioana M; Mixich VA
Forensic Sci Int; 2004 Dec; 146 Suppl():S159-61. PubMed ID: 15639566
[TBL] [Abstract][Full Text] [Related]
8. [Observation and analysis on mutation of routine STR locus].
Li QY; Feng WJ; Yang QG
Fa Yi Xue Za Zhi; 2005 May; 21(2):86-9. PubMed ID: 15931744
[TBL] [Abstract][Full Text] [Related]
9. [Mutations of short tandem repeat loci in Identifiler system].
Zhao ZM; Liu Y; Lin Y
Fa Yi Xue Za Zhi; 2007 Aug; 23(4):290-1, 294. PubMed ID: 17896523
[TBL] [Abstract][Full Text] [Related]
10. Multistep microsatellite mutation leading to father-child mismatch of FGA locus in a case of non-exclusion parentage.
Jia YS; Zhang L; Qi LY; Mei K; Zhou FL; Huang DX; Yi SH
Leg Med (Tokyo); 2015 Sep; 17(5):364-5. PubMed ID: 25979606
[TBL] [Abstract][Full Text] [Related]
11. [Allelic variant 6' at locus D13S317 in a paternity casework; a semi-automatic genotyping problem].
Opolska-Bogusz B; Kaczmarczyk G; Piniewska D; Stawowiak A; Sanak M
Arch Med Sadowej Kryminol; 2006; 56(2):115-8. PubMed ID: 16970084
[TBL] [Abstract][Full Text] [Related]
12. Identification of a novel A1v-O1v hybrid allele with G829A mutation in a chimeric individual of AelBel phenotype.
Sun CF; Chen DP; Tseng CP; Wang WT; Liu JP
Transfusion; 2006 May; 46(5):780-9. PubMed ID: 16686846
[TBL] [Abstract][Full Text] [Related]
13. [A rare D19S433*7 variant in the paternity case with mutation].
Czarnogórska M; Sanak M; Piniewska D; Kochmańska N; Stawowiak A; Opolska-Bogusz B
Arch Med Sadowej Kryminol; 2009; 59(4):320-5. PubMed ID: 20860305
[TBL] [Abstract][Full Text] [Related]
14. Multistep microsatellite mutation in the maternally transmitted locus D13S317: a case of maternal allele mismatch in the child.
Singh Negi D; Alam M; Bhavani SA; Nagaraju J
Int J Legal Med; 2006 Sep; 120(5):286-92. PubMed ID: 16514543
[TBL] [Abstract][Full Text] [Related]
15. Paternal exclusion: allele sharing in microsatellite testing.
Narkuti V; Vellanki RN; Oraganti NM; Mangamoori LN
Clin Chem Lab Med; 2008; 46(11):1586-8. PubMed ID: 19012523
[TBL] [Abstract][Full Text] [Related]
16. Triallelic patterns in STR loci used for paternity analysis: evidence for a duplication in chromosome 2 containing the TPOX STR locus.
Lukka M; Tasa G; Ellonen P; Moilanen K; Vassiljev V; Ulmanen I
Forensic Sci Int; 2006 Dec; 164(1):3-9. PubMed ID: 16337759
[TBL] [Abstract][Full Text] [Related]
17. DNA analysis in disputed parentage: the occurrence of two apparently false exclusions of paternity, both at short tandem repeat (STR) loci, in the one child.
Gunn PR; Trueman K; Stapleton P; Klarkowski DB
Electrophoresis; 1997 Aug; 18(9):1650-2. PubMed ID: 9378139
[TBL] [Abstract][Full Text] [Related]
18. The structure of a variant allele which is considered to be 30.3 in the STR locus D21S11.
Tsuji A; Ishiko A; Ikeda N
Leg Med (Tokyo); 2006 May; 8(3):182-3. PubMed ID: 16515880
[TBL] [Abstract][Full Text] [Related]
19. Possible pitfalls in motherless paternity analysis with related putative fathers.
von Wurmb-Schwark N; Mályusz V; Simeoni E; Lignitz E; Poetsch M
Forensic Sci Int; 2006 Jun; 159(2-3):92-7. PubMed ID: 16143476
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of population variation at 17 autosomal STR and 16 Y-STR haplotype loci in Croatians.
Haliti N; Carapina M; Masić M; Strinović D; Klarić IM; Kubat M
Forensic Sci Int Genet; 2009 Sep; 3(4):e137-8. PubMed ID: 19647700
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
