BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 21324748)

  • 1. First systematic experience of preimplantation genetic diagnosis for de-novo mutations.
    Rechitsky S; Pomerantseva E; Pakhalchuk T; Pauling D; Verlinsky O; Kuliev A
    Reprod Biomed Online; 2011 Apr; 22(4):350-61. PubMed ID: 21324748
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.
    Altarescu G; Eldar-Geva T; Varshower I; Brooks B; Haran EZ; Margalioth EJ; Levy-Lahad E; Renbaum P
    Hum Reprod; 2009 Dec; 24(12):3225-9. PubMed ID: 19687056
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Single-sperm analysis for haplotype construction of de-novo paternal mutations: application to PGD for neurofibromatosis type 1.
    Altarescu G; Brooks B; Kaplan Y; Eldar-Geva T; Margalioth EJ; Levy-Lahad E; Renbaum P
    Hum Reprod; 2006 Aug; 21(8):2047-51. PubMed ID: 16740526
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Three hundred and thirty cycles of preimplantation genetic diagnosis for serious genetic disease: clinical considerations affecting outcome.
    Grace J; El-Toukhy T; Scriven P; Ogilvie C; Pickering S; Lashwood A; Flinter F; Khalaf Y; Braude P
    BJOG; 2006 Dec; 113(12):1393-401. PubMed ID: 17176278
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polar body-based preimplantation genetic diagnosis for N-acetylglutamate synthase deficiency.
    Altarescu G; Brooks B; Eldar-Geva T; Margalioth EJ; Singer A; Levy-Lahad E; Renbaum P
    Fetal Diagn Ther; 2008; 24(3):170-6. PubMed ID: 18753752
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Strategies and clinical outcome of 250 cycles of Preimplantation Genetic Diagnosis for single gene disorders.
    Fiorentino F; Biricik A; Nuccitelli A; De Palma R; Kahraman S; Iacobelli M; Trengia V; Caserta D; Bonu MA; Borini A; Baldi M
    Hum Reprod; 2006 Mar; 21(3):670-84. PubMed ID: 16311287
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndrome.
    Fassihi H; Grace J; Lashwood A; Whittock NV; Braude PR; Pickering SJ; McGrath JA
    Br J Dermatol; 2006 Mar; 154(3):546-50. PubMed ID: 16445790
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preimplantation genetic diagnosis: state of the art.
    Basille C; Frydman R; El Aly A; Hesters L; Fanchin R; Tachdjian G; Steffann J; LeLorc'h M; Achour-Frydman N
    Eur J Obstet Gynecol Reprod Biol; 2009 Jul; 145(1):9-13. PubMed ID: 19411132
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation.
    Wu CC; Lin SY; Su YN; Fang MY; Chen SU; Hsu CJ
    Audiol Neurootol; 2010; 15(5):311-7. PubMed ID: 20160438
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Preimplantation genetic haplotyping: 127 diagnostic cycles demonstrating a robust, efficient alternative to direct mutation testing on single cells.
    Renwick P; Trussler J; Lashwood A; Braude P; Ogilvie CM
    Reprod Biomed Online; 2010 Apr; 20(4):470-6. PubMed ID: 20144563
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PGD for germline mosaicism.
    Altarescu G; Beeri R; Eldar-Geva T; Varshaver I; Margalioth EJ; Levy-Lahad E; Renbaum P
    Reprod Biomed Online; 2012 Oct; 25(4):390-5. PubMed ID: 22884613
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PGD on a recombinant allele: crossover between the TSC2 gene and 'linked' markers impairs accurate diagnosis.
    Altarescu G; Eldar Geva T; Brooks B; Margalioth E; Levy-Lahad E; Renbaum P
    Prenat Diagn; 2008 Oct; 28(10):929-33. PubMed ID: 18792920
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The clinical application of single-sperm-based SNP haplotyping for PGD of osteogenesis imperfecta.
    Chen L; Diao Z; Xu Z; Zhou J; Yan G; Sun H
    Syst Biol Reprod Med; 2019 Feb; 65(1):75-80. PubMed ID: 29764212
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Preimplantation genetic diagnosis for haematologic conditions.
    El-Toukhy T; Bickerstaff H; Meller S
    Curr Opin Pediatr; 2010 Feb; 22(1):28-34. PubMed ID: 19949337
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
    Malcov M; Ben-Yosef D; Schwartz T; Mey-Raz N; Azem F; Lessing JB; Amit A; Yaron Y
    Prenat Diagn; 2005 Dec; 25(13):1200-5. PubMed ID: 16353285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blastocyst preimplantation genetic diagnosis (PGD) of a mitochondrial DNA disorder.
    Treff NR; Campos J; Tao X; Levy B; Ferry KM; Scott RT
    Fertil Steril; 2012 Nov; 98(5):1236-40. PubMed ID: 22921075
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Preimplantation genetic diagnosis: twenty years of practice.
    Iwarsson E; Malmgren H; Blennow E
    Semin Fetal Neonatal Med; 2011 Apr; 16(2):74-80. PubMed ID: 21176890
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene.
    Moutou C; Machev N; Gardes N; Viville S
    Prenat Diagn; 2006 Nov; 26(11):1037-41. PubMed ID: 16941715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].
    de Die-Smulders CE; Land JA; Dreesen JC; Coonen E; Evers JL; Geraedts JP
    Ned Tijdschr Geneeskd; 2004 Dec; 148(50):2491-6. PubMed ID: 15638197
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.
    Malcov M; Reches A; Ben-Yosef D; Cohen T; Amit A; Dgany O; Tamary H; Yaron Y
    Prenat Diagn; 2010 Mar; 30(3):207-11. PubMed ID: 20049848
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.