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 *

205 related articles for article (PubMed ID: 8088823)

  • 1. Determination of gene dosage by a quantitative adaptation of the polymerase chain reaction (gd-PCR): rapid detection of deletions and duplications of gene sequences.
    Celi FS; Cohen MM; Antonarakis SE; Wertheimer E; Roth J; Shuldiner AR
    Genomics; 1994 May; 21(2):304-10. PubMed ID: 8088823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A large-scale validation of dosage analysis by robust dosage-polymerase chain reaction.
    Nguyen VQ; Liu Q; Sommer SS
    Anal Biochem; 2007 Dec; 371(1):37-42. PubMed ID: 17910884
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).
    Shi J; Shibayama A; Liu Q; Nguyen VQ; Feng J; Santos M; Temudo T; Maciel P; Sommer SS
    Hum Mutat; 2005 May; 25(5):505. PubMed ID: 15841480
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Use of multiplex PCR and CE for gene dosage quantification and its biomedical applications for SMN, PMP22, and alpha-globin genes.
    Hung CC; Chien SC; Lin CY; Chang CH; Chang YF; Jong YJ; Hsieh ST; Hsieh WS; Liu MS; Lin WL; Lee CN; Su YN
    Electrophoresis; 2007 Aug; 28(16):2826-34. PubMed ID: 17640091
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia.
    Cantafora A; Blotta I; Pino E; Pisciotta L; Calandra S; Bertolini S
    Electrophoresis; 2004 Nov; 25(21-22):3882-9. PubMed ID: 15565673
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The detection of large deletions or duplications in genomic DNA.
    Armour JA; Barton DE; Cockburn DJ; Taylor GR
    Hum Mutat; 2002 Nov; 20(5):325-37. PubMed ID: 12402329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status.
    Mansfield ES; Blasband A; Kronick MN; Wrabetz L; Kaplan P; Rappaport E; Sartore M; Parrella T; Surrey S; Fortina P
    Mol Cell Probes; 1993 Aug; 7(4):311-24. PubMed ID: 8232348
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
    Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Detection of RB1 mutations by using quantitative fluorescent mutiplex PCR].
    Du C; Gallie BL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):386-9. PubMed ID: 10581351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sensitive detection of deletions of one or more exons in the neurofibromatosis type 2 (NF2) gene by multiplexed gene dosage polymerase chain reaction.
    Diebold R; Bartelt-Kirbach B; Evans DG; Kaufmann D; Hanemann CO
    J Mol Diagn; 2005 Feb; 7(1):97-104. PubMed ID: 15681480
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
    Boehm D; Herold S; Kuechler A; Liehr T; Laccone F
    Hum Mutat; 2004 Apr; 23(4):368-78. PubMed ID: 15024731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients.
    Duponchel C; Di Rocco C; Cicardi M; Tosi M
    Hum Mutat; 2001; 17(1):61-70. PubMed ID: 11139243
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid detection of trisomy 21 by gene dosage analysis using quantitative real-time polymerase chain reaction.
    Tsujie T; Takemura M; Kimura T; Shimoya K; Tsutsui T; Ogita K; Ozaki M; Murata Y
    J Obstet Gynaecol Res; 2006 Aug; 32(4):368-72. PubMed ID: 16882261
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of heterozygous large deletions in the antithrombin gene using multiplex polymerase chain reaction and denatured high performance liquid chromatography.
    Pavlova A; El-Maarri O; Luxembourg B; Lindhoff-Last E; Kochhan L; Bruhn HD; Delev D; Watzka M; Seifried E; Oldenburg J
    Haematologica; 2006 Sep; 91(9):1264-7. PubMed ID: 16956830
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments.
    Casilli F; Di Rocco ZC; Gad S; Tournier I; Stoppa-Lyonnet D; Frebourg T; Tosi M
    Hum Mutat; 2002 Sep; 20(3):218-26. PubMed ID: 12203994
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous large deletions of Factor 8 gene in females identified by multiplex PCR-LC.
    Pavlova A; Förster T; Delev D; Schröder J; El-Maarri O; Müller-Reible C; Oldenburg J
    Haemophilia; 2008 May; 14(3):599-606. PubMed ID: 18218012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplications and de novo deletions of the SMNt gene demonstrated by fluorescence-based carrier testing for spinal muscular atrophy.
    Chen KL; Wang YL; Rennert H; Joshi I; Mills JK; Leonard DG; Wilson RB
    Am J Med Genet; 1999 Aug; 85(5):463-9. PubMed ID: 10405443
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A method for accurate detection of genomic microdeletions using real-time quantitative PCR.
    Weksberg R; Hughes S; Moldovan L; Bassett AS; Chow EW; Squire JA
    BMC Genomics; 2005 Dec; 6():180. PubMed ID: 16351727
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of unknown deletions in beta-globin gene cluster using relative quantitative PCR methods.
    Babashah S; Jamali S; Mahdian R; Nosaeid MH; Karimipoor M; Alimohammadi R; Raeisi M; Maryami F; Masoudifar M; Zeinali S
    Eur J Haematol; 2009 Sep; 83(3):261-9. PubMed ID: 19341428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.