BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 27441947)

  • 1. The impact of mosaicism in preimplantation genetic diagnosis (PGD): approaches to PGD for dominant disorders in couples without family history.
    Naja RP; Dhanjal S; Doshi A; Serhal P; Delhanty J; SenGupta SB
    Prenat Diagn; 2016 Sep; 36(9):864-70. PubMed ID: 27441947
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Preimplantation genetic diagnosis for neurofibromatosis type 1.
    Spits C; De Rycke M; Van Ranst N; Joris H; Verpoest W; Lissens W; Devroey P; Van Steirteghem A; Liebaers I; Sermon K
    Mol Hum Reprod; 2005 May; 11(5):381-7. PubMed ID: 15833774
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Preimplantation diagnosis for neurofibromatosis.
    Verlinsky Y; Rechitsky S; Verlinsky O; Chistokhina A; Sharapova T; Masciangelo C; Levy M; Kaplan B; Lederer K; Kuliev A
    Reprod Biomed Online; 2002; 4(3):218-22. PubMed ID: 12709270
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletions.
    Vanneste E; Melotte C; Debrock S; D'Hooghe T; Brems H; Fryns JP; Legius E; Vermeesch JR
    Hum Reprod; 2009 Jun; 24(6):1522-8. PubMed ID: 19278970
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Germline mosaicism is a pitfall in PGD for X-linked disorders. Single sperm typing detects very low frequency paternal gonadal mosaicism in a case of recurrent chondrodysplasia punctata misattributed to a maternal origin.
    Viart V; Willems M; Ishmukhametova A; Dufernez F; Anahory T; Hamamah S; Schmitt S; Claustres M; Girardet A
    Prenat Diagn; 2017 Feb; 37(2):201-205. PubMed ID: 27943351
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Outcomes of preimplantation genetic diagnosis in neurofibromatosis type 1.
    Merker VL; Murphy TP; Hughes JB; Muzikansky A; Hughes MR; Souter I; Plotkin SR
    Fertil Steril; 2015 Mar; 103(3):761-8.e1. PubMed ID: 25557241
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches.
    Laurie AD; Hill AM; Harraway JR; Fellowes AP; Phillipson GT; Benny PS; Smith MP; George PM
    J Thromb Haemost; 2010 Apr; 8(4):783-9. PubMed ID: 20102489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).
    Destouni A; Poulou M; Kakourou G; Vrettou C; Tzetis M; Traeger-Synodinos J; Kitsiou-Tzeli S
    J Cyst Fibros; 2016 Mar; 15(2):163-70. PubMed ID: 26493493
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Consistent and reproducible outcomes of blastocyst biopsy and aneuploidy screening across different biopsy practitioners: a multicentre study involving 2586 embryo biopsies.
    Capalbo A; Ubaldi FM; Cimadomo D; Maggiulli R; Patassini C; Dusi L; Sanges F; Buffo L; Venturella R; Rienzi L
    Hum Reprod; 2016 Jan; 31(1):199-208. PubMed ID: 26637492
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A systematic analysis of the suitability of preimplantation genetic diagnosis for mitochondrial diseases in a heteroplasmic mitochondrial mouse model.
    Neupane J; Vandewoestyne M; Heindryckx B; Ghimire S; Lu Y; Qian C; Lierman S; Van Coster R; Gerris J; Deroo T; Deforce D; De Sutter P
    Hum Reprod; 2014 Apr; 29(4):852-9. PubMed ID: 24524987
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Outcomes of trophectoderm biopsy on cryopreserved blastocysts: a case series.
    Lathi RB; Massie JA; Gilani M; Milki AA; Westphal LM; Baker VL; Behr B
    Reprod Biomed Online; 2012 Nov; 25(5):504-7. PubMed ID: 22985500
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers.
    Tan YQ; Tan K; Zhang SP; Gong F; Cheng DH; Xiong B; Lu CF; Tang XC; Luo KL; Lin G; Lu GX
    Hum Reprod; 2013 Sep; 28(9):2581-92. PubMed ID: 23847111
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reduction of the multiple pregnancy rate in a preimplantation genetic diagnosis programme after introduction of single blastocyst transfer and cryopreservation of blastocysts biopsied on day 3.
    El-Toukhy T; Kamal A; Wharf E; Grace J; Bolton V; Khalaf Y; Braude P
    Hum Reprod; 2009 Oct; 24(10):2642-8. PubMed ID: 19567414
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Parental mosaicism is a pitfall in preimplantation genetic diagnosis of dominant disorders.
    Steffann J; Michot C; Borghese R; Baptista-Fernandes M; Monnot S; Bonnefont JP; Munnich A
    Eur J Hum Genet; 2014 May; 22(5):711-2. PubMed ID: 24022303
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multicolor detection of every chromosome as a means of detecting mosaicism and nuclear organization in human embryonic nuclei.
    Turner K; Fowler K; Fonseka G; Griffin D; Ioannou D
    Panminerva Med; 2016 Jun; 58(2):175-90. PubMed ID: 26982524
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.