BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 26890253)

  • 1. Survey of prenatal testing for genetic disorders in Japan: Recent report.
    Nobuzane T; Yamada T; Miura K; Sawai H; Masuzaki H; Kudo Y
    J Obstet Gynaecol Res; 2016 Apr; 42(4):375-9. PubMed ID: 26890253
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nationwide survey for current clinical status of amniocentesis and maternal serum marker test in Japan.
    Miyake H; Yamada S; Fujii Y; Sawai H; Arimori N; Yamanouchi Y; Ozasa Y; Kanai M; Sago H; Sekizawa A; Takada F; Masuzaki H; Matsubara Y; Hirahara F; Kugu K
    J Hum Genet; 2016 Oct; 61(10):879-884. PubMed ID: 27357425
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan.
    Yotsumoto J; Sekizawa A; Suzumori N; Yamada T; Samura O; Nishiyama M; Miura K; Sawai H; Murotsuki J; Kitagawa M; Kamei Y; Masuzaki H; Hirahara F; Endo T; Fukushima A; Namba A; Osada H; Kasai Y; Watanabe A; Katagiri Y; Takeshita N; Ogawa M; Okai T; Izumi S; Hamanoue H; Inuzuka M; Haino K; Hamajima N; Nishizawa H; Okamoto Y; Nakamura H; Kanegawa T; Yoshimatsu J; Tairaku S; Naruse K; Masuyama H; Hyodo M; Kaji T; Maeda K; Matsubara K; Ogawa M; Yoshizato T; Ohba T; Kawano Y; Sago H;
    J Hum Genet; 2016 Dec; 61(12):995-1001. PubMed ID: 27604555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A nationwide genetic testing survey in Italy, year 2007.
    Dallapiccola B; Torrente I; Agolini E; Morena A; Mingarelli R
    Genet Test Mol Biomarkers; 2010 Feb; 14(1):17-22. PubMed ID: 19929427
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Patients' choices and opinions on chorionic villous sampling and non-invasive alternatives for prenatal testing following preimplantation genetic testing for hereditary disorders: A cross-sectional questionnaire study.
    Toft CLF; Diemer T; Ingerslev HJ; Pedersen IS; Adrian SW; Kesmodel US
    Prenat Diagn; 2022 Feb; 42(2):212-225. PubMed ID: 34997771
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal genetic carrier testing using triple disease screening.
    Eng CM; Schechter C; Robinowitz J; Fulop G; Burgert T; Levy B; Zinberg R; Desnick RJ
    JAMA; 1997 Oct; 278(15):1268-72. PubMed ID: 9333269
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Guidelines for genetic testing. The Japan Society of Human Genetics, Council Committee of Ethics.
    Matsuda I; Niikawa N; Sato K; Suzumori K; Fukushima Y; Fujiki N; Kanazawa I; Nakamura Y; Yonemoto S; Nakagome Y;
    J Hum Genet; 2001; 46(3):163-5. PubMed ID: 11310587
    [No Abstract]   [Full Text] [Related]  

  • 8. Beyond the Brochure: Innovations in Clinical Counseling Practices for Prenatal Genetic Testing Options.
    J Perinat Neonatal Nurs; 2019; 33(1):E1. PubMed ID: 30676460
    [No Abstract]   [Full Text] [Related]  

  • 9. Prenatal diagnosis and genetic screening--integration into prenatal care.
    Rappaport VJ
    Obstet Gynecol Clin North Am; 2008 Sep; 35(3):435-58, ix. PubMed ID: 18760229
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pre-natal genetic counseling in a resource limited country--a single center geneticist's perspectives.
    Afroze B; Jehan F
    J Pak Med Assoc; 2014 Sep; 64(9):1008-11. PubMed ID: 25823178
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Basic knowledge of genetics and genetic counseling].
    Ihara K
    Fukuoka Igaku Zasshi; 2013 Oct; 104(10):321-5. PubMed ID: 24511661
    [No Abstract]   [Full Text] [Related]  

  • 12. Prenatal screening and diagnosis for pediatricians.
    Cunniff C;
    Pediatrics; 2004 Sep; 114(3):889-94. PubMed ID: 15342871
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The utilization and outcome of diagnostic, predictive, and prenatal genetic testing for huntington disease in johannesburg, South Africa.
    Sizer EB; Haw T; Wessels TM; Kromberg JG; Krause A
    Genet Test Mol Biomarkers; 2012 Jan; 16(1):58-62. PubMed ID: 21838519
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan.
    Tanaka K; Sekijima Y; Yoshida K; Tamai M; Kosho T; Sakurai A; Wakui K; Ikeda S; Fukushima Y
    J Hum Genet; 2013 Aug; 58(8):560-3. PubMed ID: 23635952
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Noninvasive prenatal genetic diagnosis: a bioethical reflection on the use of noninvasive prenatal diagnosis from the analysis of nucleic acids present in maternal peripheral blood].
    González-Melado FJ; Di Pietro ML
    Cuad Bioet; 2011; 22(74):49-75. PubMed ID: 21692554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acceptance of prenatal diagnosis for genetic disorders in Lebanon.
    Zahed L; Nabulsi M; Bou-Ghanim M; Usta I
    Prenat Diagn; 1999 Dec; 19(12):1109-12. PubMed ID: 10590426
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Ethical requirements for genetic testing in pregnancy as well as during childhood and adolescence].
    Henn W
    Dtsch Med Wochenschr; 2008 Jan; 133(4):147-50. PubMed ID: 18197592
    [No Abstract]   [Full Text] [Related]  

  • 18. [Preimplantation diagnosis of dominant inherited diseases with late debut].
    Sørensen SA
    Ugeskr Laeger; 2000 Aug; 162(33):4371-3. PubMed ID: 10962958
    [No Abstract]   [Full Text] [Related]  

  • 19. The centralized prenatal genetics screening program of New York City III: The first 7,000 cases.
    Benn PA; Hsu LY; Carlson A; Tannenbaum HL
    Am J Med Genet; 1985 Feb; 20(2):369-84. PubMed ID: 2579556
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carrier testing for Ashkenazi Jewish disorders in the prenatal setting: navigating the genetic maze.
    Ferreira JC; Schreiber-Agus N; Carter SM; Klugman S; Gregg AR; Gross SJ
    Am J Obstet Gynecol; 2014 Sep; 211(3):197-204. PubMed ID: 24508465
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.