These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

497 related articles for article (PubMed ID: 8754581)

  • 1. Paternity exclusion by DNA markers: effects of paternal mutations.
    Chakraborty R; Stivers DN
    J Forensic Sci; 1996 Jul; 41(4):671-7. PubMed ID: 8754581
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Paternity testing: blood group systems and DNA analysis by variable number of tandem repeat markers.
    Akane A; Matsubara K; Shiono H; Yuasa I; Yokota S; Yamada M; Nakagome Y
    J Forensic Sci; 1990 Sep; 35(5):1217-25. PubMed ID: 1977840
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [Evaluation on the number and value of STR loci applied in paternity identification].
    Fang JX; Cheng DL
    Fa Yi Xue Za Zhi; 2002 Feb; 18(1):19-21. PubMed ID: 12596583
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation rates at 14 STR loci in the population from Pernambuco, Northeast Brazil.
    de Andrade ES; Gomes AV; Raposo G; Mauricio-da-Silva L; Silva Rdos S
    Forensic Sci Int Genet; 2009 Sep; 3(4):e141-3. PubMed ID: 19647702
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Rapid and efficient resolution of parentage by amplification of short tandem repeats.
    Alford RL; Hammond HA; Coto I; Caskey CT
    Am J Hum Genet; 1994 Jul; 55(1):190-5. PubMed ID: 8023845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. The relevance of paternity analysis in Romanian population using the D1S80 locus.
    Ceacăreanu AC; Ceacăreanu B
    Roum Arch Microbiol Immunol; 1999; 58(3-4):281-8. PubMed ID: 11845466
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The evaluation of Identifiler system in paternity testing].
    Que TZ; Yan PH; Lin Y; Liu Y; Li L
    Fa Yi Xue Za Zhi; 2009 Jun; 25(3):184-6. PubMed ID: 19697775
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypervariable polymorphic VNTR loci for parentage testing and individual identification.
    Yokoi T; Nata M; Odaira T; Sagisaka K
    Jinrui Idengaku Zasshi; 1990 Jun; 35(2):179-88. PubMed ID: 2398633
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Subtyping of D11S488 STR alleles by single-strand conformation polymorphism (SSCP) analysis in two cases of disputed parentage.
    Fukuda M; Tamaki Y
    Nihon Hoigaku Zasshi; 1998 Feb; 52(1):42-5. PubMed ID: 9591402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. The potential contribution of MVR-PCR to paternity probabilities in a case lacking a mother.
    Tamaki K; Huang XL; Mizutani M; Yamamoto T; Katsumata R; Uchihi R; Katsumata Y; Jeffreys AJ
    J Forensic Sci; 1999 Jul; 44(4):863-7. PubMed ID: 10432623
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 25.