BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 20102489)

  • 1. 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]  

  • 2. Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A.
    Zhao M; Chen M; Tan ASC; Cheah FSH; Mathew J; Wong PC; Chong SS
    J Thromb Haemost; 2017 Jul; 15(7):1473-1483. PubMed ID: 28345288
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A versatile strategy for preimplantation genetic diagnosis of haemophilia A based on F8-gene sequencing.
    Sánchez-García JF; Gallardo D; Navarro J; Márquez C; Gris JM; Sánchez MA; Altisent C; Vidal F
    Thromb Haemost; 2006 Dec; 96(6):839-45. PubMed ID: 17139381
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Experience of Preimplantation Genetic Diagnosis for Hemophilia at the University Hospital Virgen Del Rocío in Spain: Technical and Clinical Overview.
    Fernández RM; Peciña A; Sánchez B; Lozano-Arana MD; García-Lozano JC; Pérez-Garrido R; Núñez R; Borrego S; Antiñolo G
    Biomed Res Int; 2015; 2015():406096. PubMed ID: 26258137
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic diagnosis in Hemophilia A from southern China: five novel mutations and one preimplantation genetic analysis.
    Chen J; Wang J; Lin XY; Xu YW; He ZH; Li HY; Chen SQ; Jiang WY
    Int J Lab Hematol; 2017 Apr; 39(2):191-201. PubMed ID: 27868395
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Live birth following the first mutation specific pre-implantation genetic diagnosis for haemophilia A.
    Michaelides K; Tuddenham EG; Turner C; Lavender B; Lavery SA
    Thromb Haemost; 2006 Feb; 95(2):373-9. PubMed ID: 16493501
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Application study on inversion diagnosis of F8 gene in hemophilia A].
    Qi LY; Jin CL; Lin CK; Ren MH; Dong WH; Sun KL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):405-8. PubMed ID: 17680530
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Introns 1 and 22 inversions and F8 gene sequencing for molecular diagnosis of hemophilia A in Chile].
    Poggi H; Honorato J; Romeo E; Zúñiga P; Quiroga T; Lagos M
    Rev Med Chil; 2011 Feb; 139(2):189-96. PubMed ID: 21773656
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiplex fluorescent analysis of four short tandem repeats for rapid haemophilia A molecular diagnosis.
    Sánchez-García JF; Gallardo D; Ramírez L; Vidal F
    Thromb Haemost; 2005 Nov; 94(5):1099-103. PubMed ID: 16363255
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Preimplantation genetic testing (PGT) for hemophilia A: Experience from one center.
    Bui TMP; Tran VK; Nguyen TTH; Le TP; Nguyen TM; Tran HA; Luu VD; Nguyen MH; Bui TH; Van Ta T; Tran TH
    Taiwan J Obstet Gynecol; 2022 Nov; 61(6):1009-1014. PubMed ID: 36427965
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesis.
    Chen C; Xie X; Wu X; Lu Y; Wang X; Wu W; Hu Y; Ding Q
    Thromb Haemost; 2017 Jul; 117(8):1478-1485. PubMed ID: 28492696
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotyping of intron 22 inversion of factor VIII gene for diagnosis of hemophilia A by inverse-shifting polymerase chain reaction and capillary electrophoresis.
    Pan TY; Wang CC; Shih CJ; Wu HF; Chiou SS; Wu SM
    Anal Bioanal Chem; 2014 Sep; 406(22):5447-54. PubMed ID: 24994666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole F8 gene sequencing identified pathogenic structural variants in the remaining unsolved patients with severe hemophilia A.
    Jourdy Y; Chatron N; Frétigny M; Zawadzki C; Lienhart A; Stieltjes N; Rohrlich PS; Thauvin-Robinet C; Volot F; Hamida YF; Hariti G; Leuci A; Dargaud Y; Sanlaville D; Vinciguerra C
    J Thromb Haemost; 2024 Jun; 22(6):1616-1626. PubMed ID: 38484912
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV.
    De Vos A; Sermon K; Van de Velde H; Joris H; Vandervorst M; Lissens W; De Paepe A; Liebaers I; Van Steirteghem A
    Hum Genet; 2000 Jun; 106(6):605-13. PubMed ID: 10942108
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotyping of intron 22-related rearrangements of F8 by inverse-shifting PCR in Egyptian hemophilia A patients.
    Abou-Elew H; Ahmed H; Raslan H; Abdelwahab M; Hammoud R; Mokhtar D; Arnaout H
    Ann Hematol; 2011 May; 90(5):579-84. PubMed ID: 21072517
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line.
    Altarescu G; Renbaum P; Eldar-Geva T; Brooks B; Varshaver I; Avitzour M; Margalioth EJ; Levy-Lahad E; Elstein D; Epsztejn-Litman S; Eiges R
    Prenat Diagn; 2011 Sep; 31(9):853-60. PubMed ID: 21706504
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aberrant F8 gene intron 1 inversion with concomitant duplication and deletion in a severe hemophilia A patient from Southern Italy.
    Sanna V; Ceglia C; Tarsitano M; Lombardo B; Coppola A; Zarrilli F; Castaldo G; Di Minno G
    J Thromb Haemost; 2013 Jan; 11(1):195-7. PubMed ID: 23140572
    [No Abstract]   [Full Text] [Related]  

  • 18. Inverse PCR to perform long-distance haplotyping: main applications to improve preimplantation genetic diagnosis in hemophilia.
    Abelleyro MM; Marchione VD; Palmitelli M; Radic CP; Neme D; Larripa IB; Medina-Acosta E; De Brasi CD; Rossetti LC
    Eur J Hum Genet; 2019 Apr; 27(4):603-611. PubMed ID: 30626931
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A.
    Bagnall RD; Waseem N; Green PM; Giannelli F
    Blood; 2002 Jan; 99(1):168-74. PubMed ID: 11756167
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations.
    Elmahmoudi H; Khodjet-el-khil H; Wigren E; Jlizi A; Zahra K; Pellechia D; Vinciguerra C; Meddeb B; Elggaaied AB; Gouider E
    Diagn Pathol; 2012 Aug; 7():93. PubMed ID: 22883072
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.