메뉴 건너뛰기




Volumn 129, Issue 3, 2017, Pages e35-e40

Carrier screening in the age of genomic medicine
[No Author Info available]

Author keywords

[No Author keywords available]

Indexed keywords

GENETIC COUNSELING; GENETIC SCREENING; GENOME; HETEROZYGOTE; HUMAN; PRENATAL SCREENING; PREPREGNANCY CARE; PRIORITY JOURNAL; REVIEW; ETHNIC GROUP; FEMALE; GENETICS; GENOMICS; HETEROZYGOTE DETECTION; PRACTICE GUIDELINE; PREGNANCY; PRENATAL DIAGNOSIS; PROCEDURES;

EID: 85015825333     PISSN: 00297844     EISSN: 1873233X     Source Type: Journal    
DOI: 10.1097/AOG.0000000000001951     Document Type: Review
Times cited : (191)

References (9)
  • 1
    • 84987668863 scopus 로고    scopus 로고
    • Modeled fetal risk of genetic diseases identified by expanded carrier screening
    • [PubMed]
    • Haque IS, Lazarin GA, Kang HP, Evans EA, Goldberg JD, Wapner RJ. Modeled fetal risk of genetic diseases identified by expanded carrier screening. JAMA 2016;316:734-42. [PubMed]
    • (2016) JAMA , vol.316 , pp. 734-742
    • Haque, I.S.1    Lazarin, G.A.2    Kang, H.P.3    Evans, E.A.4    Goldberg, J.D.5    Wapner, R.J.6
  • 2
    • 84923584486 scopus 로고    scopus 로고
    • Expanded carrier screening in reproductive medicine-points to consider: A joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine
    • [PubMed] [Obstetrics & Gynecology]
    • Edwards JG, Feldman G, Goldberg J, Gregg AR, Norton ME, Rose NC, et al. Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine. Obstet Gynecol 2015;125:653-62. [PubMed] [Obstetrics & Gynecology]
    • (2015) Obstet Gynecol , vol.125 , pp. 653-662
    • Edwards, J.G.1    Feldman, G.2    Goldberg, J.3    Gregg, A.R.4    Norton, M.E.5    Rose, N.C.6
  • 3
    • 84925032846 scopus 로고    scopus 로고
    • Newborn screening and the role of the obstetrician-gynecologist. Committee Opinion No. 616. American College of Obstetricians and Gynecologists
    • [PubMed] [Obstetrics & Gynecology]
    • Newborn screening and the role of the obstetrician-gynecologist. Committee Opinion No. 616. American College of Obstetricians and Gynecologists. Obstet Gynecol 2015;125:256-60. [PubMed] [Obstetrics & Gynecology]
    • (2015) Obstet Gynecol , vol.125 , pp. 256-260
  • 4
    • 47749092841 scopus 로고    scopus 로고
    • Ethical issues in genetic testing. ACOG Committee Opinion No. 410. American College of Obstetricians and Gynecologists
    • [PubMed] [Obstetrics & Gynecology]
    • Ethical issues in genetic testing. ACOG Committee Opinion No. 410. American College of Obstetricians and Gynecologists. Obstet Gynecol 2008;111:1495-502. [PubMed] [Obstetrics & Gynecology]
    • (2008) Obstet Gynecol , vol.111 , pp. 1495-1502
  • 5
    • 84874584838 scopus 로고    scopus 로고
    • Committee on Bioethics, Committee on Genetics, and the American College of Medical Genetics and Genomics Social, Ethical, and Legal Issues Committee
    • [PubMed]
    • Ethical and policy issues in genetic testing and screening of children. Committee on Bioethics, Committee on Genetics, and the American College of Medical Genetics and Genomics Social, Ethical, and Legal Issues Committee. Pediatrics 2013;131:620-2. [PubMed]
    • (2013) Pediatrics , vol.131 , pp. 620-622
  • 6
    • 84984830666 scopus 로고    scopus 로고
    • Where to draw the boundaries for prenatal carrier screening
    • [PubMed]
    • Grody WW. Where to draw the boundaries for prenatal carrier screening. JAMA 2016;316:717-9. [PubMed]
    • (2016) JAMA , vol.316 , pp. 717-719
    • Grody, W.W.1
  • 7
    • 84963533561 scopus 로고    scopus 로고
    • NGS-based assay for the identification of individuals carrying recessive genetic mutations in reproductive medicine
    • [PubMed] [Full Text]
    • Abuli A, Boada M, Rodriguez-Santiago B, Coroleu B, Veiga A, Armengol L, et al. NGS-based assay for the identification of individuals carrying recessive genetic mutations in reproductive medicine. Hum Mutat 2016;37:516-23. [PubMed] [Full Text]
    • (2016) Hum Mutat , vol.37 , pp. 516-523
    • Abuli, A.1    Boada, M.2    Rodriguez-Santiago, B.3    Coroleu, B.4    Veiga, A.5    Armengol, L.6
  • 8
    • 84945910426 scopus 로고    scopus 로고
    • Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology
    • [PubMed] [Full Text]
    • Martin J, Asan, Yi Y, Alberola T, Rodriguez-Iglesias B, Jimenez-Almazan J, et al. Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology. Fertil Steril 2015;104:1286-93. [PubMed] [Full Text]
    • (2015) Fertil Steril , vol.104 , pp. 1286-1293
    • Martin, J.1    Asan Yi, Y.2    Alberola, T.3    Rodriguez-Iglesias, B.4    Jimenez-Almazan, J.5
  • 9
    • 85026563797 scopus 로고    scopus 로고
    • Carrier screening for genetic conditions. Committee Opinion No. 691. American College of Obstetricians and Gynecologists
    • Carrier screening for genetic conditions. Committee Opinion No. 691. American College of Obstetricians and Gynecologists. Obstet Gynecol 2017;129:e41-55.
    • (2017) Obstet Gynecol , vol.129 , pp. e41-55


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.