메뉴 건너뛰기




Volumn 87, Issue 22, 2007, Pages 1540-1544

Prenatal gene diagnosis of paternally inherited α-thalassemia by detecting fetal DNA in maternal plasma

Author keywords

Alpha thalassemia; Fetal DNA; Maternal plasma; Prenatal diagnosis

Indexed keywords

DNA;

EID: 34548245028     PISSN: 03762491     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (14)
  • 1
    • 0342618532 scopus 로고    scopus 로고
    • Presence of fetal DNA in maternal plasma and serum
    • Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet, 1997, 350: 485-487.
    • (1997) Lancet , vol.350 , pp. 485-487
    • YM, L.1    Corbetta, N.2    Chamberlain, P.F.3
  • 2
    • 0032506669 scopus 로고    scopus 로고
    • Prenatal diagnosis of fetal RhD status by molecular analysis of materal plasma
    • Lo YM, Hjelm NM, Fidler C, et al. Prenatal diagnosis of fetal RhD status by molecular analysis of materal plasma. N Engl J Med, 1998, 339: 1734-1738.
    • (1998) N Engl J Med , vol.339 , pp. 1734-1738
    • YM, L.1    Hjelm, N.M.2    Fidler, C.3
  • 3
    • 0034715975 scopus 로고    scopus 로고
    • Prenatal detection of fetal Down's syndrome from maternal plasma
    • Poon LL, Leung TN, Lau TK, et al. Prenatal detection of fetal Down's syndrome from maternal plasma. Lancet, 2000, 356: 1819-1820.
    • (2000) Lancet , vol.356 , pp. 1819-1820
    • Poon, L.L.1    Leung, T.N.2    Lau, T.K.3
  • 4
    • 0037190608 scopus 로고    scopus 로고
    • Prenatal exclusion of β-thalassaemia major by examination of maternal plasma
    • Chiu RW, Lau TK, Leung TN, et al. Prenatal exclusion of β-thalassaemia major by examination of maternal plasma. Lancet, 2002, 360: 998-1000.
    • (2002) Lancet , vol.360 , pp. 998-1000
    • Chiu, R.W.1    Lau, T.K.2    Leung, T.N.3
  • 5
    • 13844269123 scopus 로고    scopus 로고
    • Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionted cell-free DNA in maternal plasma
    • Li Y, Di Naro E, Vitucci A, et al. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionted cell-free DNA in maternal plasma. JAMA, 2005, 293: 843-849.
    • (2005) JAMA , vol.293 , pp. 843-849
    • Li, Y.1    Di Naro, E.2    Vitucci, A.3
  • 6
    • 0037903707 scopus 로고    scopus 로고
    • Prenatal detection of fetal hemeoglobin E gene from maternal plasma
    • Fucharoen G, Tungwiwat W, Ratanasiri T, et al. Prenatal detection of fetal hemeoglobin E gene from maternal plasma. Prenat Diagn, 2003, 23: 393-396.
    • (2003) Prenat Diagn , vol.23 , pp. 393-396
    • Fucharoen, G.1    Tungwiwat, W.2    Ratanasiri, T.3
  • 7
    • 3242703837 scopus 로고    scopus 로고
    • MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis
    • Ding C, Chiu RW, Lau TK. MS analysis of single-nucleotide differences in circulating nucleic acids: application to noninvasive prenatal diagnosis. Proc Natl Acad Sci USA, 2004, 101: 10762-10767.
    • (2004) Proc Natl Acad Sci USA , vol.101 , pp. 10762-10767
    • Ding, C.1    Chiu, R.W.2    Lau, T.K.3
  • 8
    • 0347898005 scopus 로고    scopus 로고
    • Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis
    • Lo YM, Tein MS, Lau TK, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet, 1998, 62:768-775.
    • (1998) Am J Hum Genet , vol.62 , pp. 768-775
    • YM, L.1    Tein, M.S.2    Lau, T.K.3
  • 9
    • 34548203119 scopus 로고    scopus 로고
    • Chinese source.
    • Chinese source.
  • 11
    • 34548211344 scopus 로고    scopus 로고
    • Huisman TH, Carver MF, Baysal E. The α-thalassemia alleles//Huisman TH, Carver MF, Baysal E. A syllabus of thalassemia mutations. Augusta: The Sickle Cell Anemia Foundation, 1997: 235-296.
    • Huisman TH, Carver MF, Baysal E. The α-thalassemia alleles//Huisman TH, Carver MF, Baysal E. A syllabus of thalassemia mutations. Augusta: The Sickle Cell Anemia Foundation, 1997: 235-296.
  • 12
    • 0034818672 scopus 로고    scopus 로고
    • Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia
    • Rijnders RJ, van der Schoot CE, Bossers B, et al. Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia. Obstet-Gynecol, 2001, 98: 374-378.
    • (2001) Obstet-Gynecol , vol.98 , pp. 374-378
    • Rijnders, R.J.1    van der Schoot, C.E.2    Bossers, B.3
  • 13
    • 0034016272 scopus 로고    scopus 로고
    • Detection of male and female fetal DNA in maternal plasma by multiplex fluorescent polymerase chain reaction amplification of short tandem repeats
    • Pertl B, Sekizawa A, Samura O, et al. Detection of male and female fetal DNA in maternal plasma by multiplex fluorescent polymerase chain reaction amplification of short tandem repeats. Hum Genet, 2000, 106: 45-49.
    • (2000) Hum Genet , vol.106 , pp. 45-49
    • Pertl, B.1    Sekizawa, A.2    Samura, O.3
  • 14
    • 0032754195 scopus 로고    scopus 로고
    • Detection of fetal-derived paternally inherited X-chromosome polymorphisms in maternal plasma
    • Tang NL, Leung TN, Zhang J, et al. Detection of fetal-derived paternally inherited X-chromosome polymorphisms in maternal plasma. Clin Chem, 1999, 45: 2033-2035.
    • (1999) Clin Chem , vol.45 , pp. 2033-2035
    • Tang, N.L.1    Leung, T.N.2    Zhang, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.