메뉴 건너뛰기




Volumn 314, Issue 20, 2015, Pages 2192-

Maternal malignancies detected with noninvasive prenatal testing

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME 8; COPY NUMBER VARIATION; GENETIC ALGORITHM; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENOTYPE; HUMAN; INCIDENTAL FINDING; LETTER; MALIGNANT NEOPLASTIC DISEASE; MATERNAL DISEASE; MONOSOMY; NON INVASIVE PROCEDURE; PREGNANT WOMAN; PRENATAL SCREENING; PRIORITY JOURNAL; X CHROMOSOME; Y CHROMOSOME; ANEUPLOIDY; BLOOD; CHROMOSOME DISORDERS; FEMALE; GENETIC SCREENING; GENETICS; NEOPLASM; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84948153128     PISSN: 00987484     EISSN: 15383598     Source Type: Journal    
DOI: 10.1001/jama.2015.12922     Document Type: Letter
Times cited : (5)

References (5)
  • 1
    • 84937459187 scopus 로고    scopus 로고
    • Noninvasive prenatal testing and incidental detection of occult maternal malignancies
    • Bianchi DW, Chudova D, Sehnert AJ, et al. Noninvasive prenatal testing and incidental detection of occult maternal malignancies. JAMA. 2015;314(2):162-169.
    • (2015) JAMA , vol.314 , Issue.2 , pp. 162-169
    • Bianchi, D.W.1    Chudova, D.2    Sehnert, A.J.3
  • 2
    • 84899014645 scopus 로고    scopus 로고
    • WISECONDOR: Detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme
    • Straver R, Sistermans EA, Holstege H, Visser A, Oudejans CB, Reinders MJ. WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme. Nucleic Acids Res. 2014; 42(5):e31.
    • (2014) Nucleic Acids Res , vol.42 , Issue.5 , pp. e31
    • Straver, R.1    Sistermans, E.A.2    Holstege, H.3    Visser, A.4    Oudejans, C.B.5    Reinders, M.J.6
  • 3
    • 84901253329 scopus 로고    scopus 로고
    • Introducing WISECONDOR for noninvasive prenatal diagnostics
    • Straver R, Sistermans EA, Reinders MJ. Introducing WISECONDOR for noninvasive prenatal diagnostics. Expert Rev Mol Diagn. 2014;14(5):513-515.
    • (2014) Expert Rev Mol Diagn , vol.14 , Issue.5 , pp. 513-515
    • Straver, R.1    Sistermans, E.A.2    Reinders, M.J.3
  • 4
    • 84919935832 scopus 로고    scopus 로고
    • Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories
    • Thung DT, Beulen L, Hehir-Kwa J, Faas BH. Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories. Expert Rev Mol Diagn. 2015;15(1):111-124.
    • (2015) Expert Rev Mol Diagn , vol.15 , Issue.1 , pp. 111-124
    • Thung, D.T.1    Beulen, L.2    Hehir-Kwa, J.3    Faas, B.H.4
  • 5
    • 84944161591 scopus 로고    scopus 로고
    • Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management
    • Bayindir B, Dehaspe L, Brison N, et al. Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management. Eur J Hum Genet. 2015;23(10):1286-1293.
    • (2015) Eur J Hum Genet , vol.23 , Issue.10 , pp. 1286-1293
    • Bayindir, B.1    Dehaspe, L.2    Brison, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.