BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 17302781)

  • 1. Assessing exclusionary power of a paternity test involving a pair of alleged grandparents.
    Scarpetta MA; Staub RW; Einum DD
    Transfusion; 2007 Feb; 47(2):335-40. PubMed ID: 17302781
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Maternal typing and test sufficiency in parentage analyses.
    Wenk RE; Houtz T; Chiafari FA
    Transfusion; 2006 Feb; 46(2):199-203. PubMed ID: 16441595
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Use of X-linked short tandem repeat loci in routine parentage casework.
    Silveira D; Silva FF; Jesus PR; Whittle MR
    Transfusion; 2007 Jun; 47(6):1050-3. PubMed ID: 17524096
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The specific power of parentage exclusion in a child's blood relatives.
    Wenk RE; Gjertson DW; Chiafari FA; Houtz T
    Transfusion; 2005 Mar; 45(3):440-4. PubMed ID: 15752164
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Chromosome STR genetic markers in paternity identification].
    Li J
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2004 Aug; 29(4):432-4. PubMed ID: 16134597
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The application of minisatellite variant repeat mapping by PCR (MVR-PCR) in a paternity case showing false exclusion due to STR mutation.
    Yamamoto T; Tamaki K; Huang XL; Yoshimoto T; Mizutani M; Uchihi R; Katsumata Y; Jeffreys AJ
    J Forensic Sci; 2001 Mar; 46(2):374-8. PubMed ID: 11305445
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [How to draw a conclusion in motherless parentage testing using short tandem repeats as genetic makers].
    Zhu YL; Huang YM; Wu XY
    Fa Yi Xue Za Zhi; 2006 Aug; 22(4):281-4. PubMed ID: 17080668
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Paternity exclusion power: comparative behaviour of autosomal and X-chromosomal markers in standard and deficient cases with inbreeding.
    Pinto N; Gusmão L; Egeland T; Amorim A
    Forensic Sci Int Genet; 2013 Feb; 7(2):290-5. PubMed ID: 23312390
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers.
    Phillips C; Fondevila M; García-Magariños M; Rodriguez A; Salas A; Carracedo A; Lareu MV
    Forensic Sci Int Genet; 2008 Jun; 2(3):198-204. PubMed ID: 19083821
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quintuplex PCR-amplification of microsatellites.
    Wang W; Fukuda M; Kishida T; Tamaki Y
    Nihon Hoigaku Zasshi; 1996 Aug; 50(4):231-6. PubMed ID: 8810743
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Genetic marker analysis in cases of disputed paternity when the alleged father is deceased.
    Smith RA; Gutendorf RW; McCloskey J
    Ann Clin Lab Sci; 1989; 19(5):332-6. PubMed ID: 2802512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Evaluation of 9 STR loci in paternity identification].
    Liu Y
    Fa Yi Xue Za Zhi; 2000 Nov; 16(4):216-8, S2. PubMed ID: 12536971
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A reference data base on STR allele frequencies in the Belarus population developed from paternity cases.
    Zhivotovsky LA; Veremeichyk VM; Kuzub NN; Atramentova LA; Udina IG; Kartel NA; Tsybovsky IS
    Forensic Sci Int Genet; 2009 Jun; 3(3):e107-9. PubMed ID: 19414154
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A study of paternity testing with considering mutation].
    Hou YP; Wu J; Hou JY; Yan J; Li YB; Gao S; Sun XM; Luo HB
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):417-21. PubMed ID: 17680532
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Probability of exclusion in paternity testing: time to reassess.
    Cifuentes LO; Martínez EH; Acuña MP; Jonquera HG
    J Forensic Sci; 2006 Mar; 51(2):349-50. PubMed ID: 16566769
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Basic concepts about paternity testing].
    Lagos M; Poggi H; Mellado C
    Rev Med Chil; 2011 Apr; 139(4):542-7. PubMed ID: 21879196
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Estimation of nonpaternity in the Mexican population of Nuevo Leon: a validation study with blood group markers.
    Cerda-Flores RM; Barton SA; Marty-Gonzalez LF; Rivas F; Chakraborty R
    Am J Phys Anthropol; 1999 Jul; 109(3):281-93. PubMed ID: 10407460
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Use of X-linked short tandem repeats loci to confirm mutations in parentage caseworks.
    Chen DP; Tseng CP; Tsai SH; Wang MC; Lu SC; Wu TL; Chang PY; Sun CF
    Clin Chim Acta; 2009 Oct; 408(1-2):29-33. PubMed ID: 19595994
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.