메뉴 건너뛰기




Volumn 60, Issue 4, 1997, Pages 917-927

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; FETUS; FETUS OUTCOME; HUMAN; HUMAN CELL; INTRAUTERINE GROWTH RETARDATION; MAJOR CLINICAL STUDY; MEIOSIS; MOSAICISM; NEWBORN; PLACENTA; PRIORITY JOURNAL; TRISOMY; TROPHOBLAST; UNIPARENTAL DISOMY;

EID: 16944367292     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (192)

References (37)
  • 1
    • 0027447719 scopus 로고
    • Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
    • Antonarakis S, Avramopoulus D, Blouin J-L, Talbot JC, Schinzel A (1993) Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age. Nat Genet 3:146-150
    • (1993) Nat Genet , vol.3 , pp. 146-150
    • Antonarakis, S.1    Avramopoulus, D.2    Blouin, J.-L.3    Talbot, J.C.4    Schinzel, A.5
  • 7
    • 0030950624 scopus 로고    scopus 로고
    • Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias and oligohydramnios
    • in press
    • Hansen WF, Bernard LE, Langlois S, Rao KW, Chescheir NC, Aylsworth AS, Smith DI, et al. Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias and oligohydramnios. Prenat Diagn (in press)
    • Prenat Diagn
    • Hansen, W.F.1    Bernard, L.E.2    Langlois, S.3    Rao, K.W.4    Chescheir, N.C.5    Aylsworth, A.S.6    Smith, D.I.7
  • 8
    • 0029077269 scopus 로고
    • Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture
    • Harrison K, Eisenger K, Anyane-Yeboa K, Brown S (1995) Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture. Am J Med Genet 58:147-151
    • (1995) Am J Med Genet , vol.58 , pp. 147-151
    • Harrison, K.1    Eisenger, K.2    Anyane-Yeboa, K.3    Brown, S.4
  • 9
    • 0029118422 scopus 로고
    • Recombination and maternal age-dependent nondisjunction: Molecular studies of trisomy 16
    • Hassold T, Merrill M, Adkins K, Freeman S, Sherman S (1995) Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. Am J Hum Genet 57: 867-874
    • (1995) Am J Hum Genet , vol.57 , pp. 867-874
    • Hassold, T.1    Merrill, M.2    Adkins, K.3    Freeman, S.4    Sherman, S.5
  • 11
    • 0030049019 scopus 로고    scopus 로고
    • Molecular studies of the aetiology of trisomy 8 in spontaneous abortions and the liveborn population
    • James RS, Jacobs PA (1996) Molecular studies of the aetiology of trisomy 8 in spontaneous abortions and the liveborn population. Hum Genet 97:283-286
    • (1996) Hum Genet , vol.97 , pp. 283-286
    • James, R.S.1    Jacobs, P.A.2
  • 12
    • 0002711242 scopus 로고
    • Mosaicism confined to chorionic tissue in human gestations
    • Fraccaro M (ed). Springer, Berlin
    • Kalousek DK (1985) Mosaicism confined to chorionic tissue in human gestations. In: Fraccaro M (ed) First trimester fetal diagnosis. Springer, Berlin, pp 130-136
    • (1985) First Trimester Fetal Diagnosis , pp. 130-136
    • Kalousek, D.K.1
  • 13
    • 0028268934 scopus 로고
    • Current topic: Confined placental mosaicism and intrauterine fetal development
    • _ (1994) Current topic: confined placental mosaicism and intrauterine fetal development. Placenta 15:219-230
    • (1994) Placenta , vol.15 , pp. 219-230
  • 14
    • 0027957179 scopus 로고
    • Confined placental mosaicism and stillbirth
    • Kalousek DK, Barrett I (1994) Confined placental mosaicism and stillbirth. Pediatr Pathol 14:151-159
    • (1994) Pediatr Pathol , vol.14 , pp. 151-159
    • Kalousek, D.K.1    Barrett, I.2
  • 15
    • 0024596935 scopus 로고
    • Placental mosaicism and intrauterine survival of trisomies 13 and 18
    • Kalousek DK, Barrett IJ, McGillivray BC (1989) Placental mosaicism and intrauterine survival of trisomies 13 and 18. Am J Hum Genet 44:338-343
    • (1989) Am J Hum Genet , vol.44 , pp. 338-343
    • Kalousek, D.K.1    Barrett, I.J.2    McGillivray, B.C.3
  • 16
    • 0020606517 scopus 로고
    • Chromosomal mosaicism confined to the placenta in human conceptions
    • Kalousek DK, Dill F (1983) Chromosomal mosaicism confined to the placenta in human conceptions. Science 221:665-667
    • (1983) Science , vol.221 , pp. 665-667
    • Kalousek, D.K.1    Dill, F.2
  • 22
    • 0028867372 scopus 로고
    • Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7
    • Langlois S, Yong SL, Wilson RD, Kwong LC, Kalousek DK (1995) Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7. J Med Genet 32:871-875
    • (1995) J Med Genet , vol.32 , pp. 871-875
    • Langlois, S.1    Yong, S.L.2    Wilson, R.D.3    Kwong, L.C.4    Kalousek, D.K.5
  • 23
    • 0029162269 scopus 로고
    • Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
    • Ledbetter DH, Engel E (1995) Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum Mol Genet 4:1757-1764
    • (1995) Hum Mol Genet , vol.4 , pp. 1757-1764
    • Ledbetter, D.H.1    Engel, E.2
  • 25
    • 0001495044 scopus 로고
    • Chromosomal findings in chorionic villi. A collaborative study
    • Vogel FS, Sperling K (eds) Springer, Berlin
    • Mikkelsen M, Ayme S (1987) Chromosomal findings in chorionic villi. A collaborative study. In: Vogel FS, Sperling K (eds) Human genetics. Springer, Berlin, pp 596-606
    • (1987) Human Genetics , pp. 596-606
    • Mikkelsen, M.1    Ayme, S.2
  • 30
    • 0028854976 scopus 로고
    • Molecular studies of chromosomal mosaicism: Relative frequency of chromosome gain or loss and possible role of cell selection
    • Robinson WP, Binkert F, Bernasconi F, Lorda-Sanchez I, Werder EA, Schinzel AA (1995) Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection. Am J Hum Genet 56:444-451
    • (1995) Am J Hum Genet , vol.56 , pp. 444-451
    • Robinson, W.P.1    Binkert, F.2    Bernasconi, F.3    Lorda-Sanchez, I.4    Werder, E.A.5    Schinzel, A.A.6
  • 33
    • 0002062341 scopus 로고
    • Discordance between prenatal cytogenetic diagnosis after chorionic villi sampling and chromosomal constitution of the fetus
    • Fraccaro MS, Brambati G (eds) Springer, Berlin
    • Simoni G (1985) Discordance between prenatal cytogenetic diagnosis after chorionic villi sampling and chromosomal constitution of the fetus. In: Fraccaro MS, Brambati G (eds) First trimester fetal diagnosis. Springer, Berlin, pp 137-143
    • (1985) First Trimester Fetal Diagnosis , pp. 137-143
    • Simoni, G.1
  • 34
    • 0028675022 scopus 로고
    • Confined placental mosaicism
    • Simoni G, Sirchia S (1994) Confined placental mosaicism. Prenat Diagn 14:1185-1189
    • (1994) Prenat Diagn , vol.14 , pp. 1185-1189
    • Simoni, G.1    Sirchia, S.2
  • 35
    • 0027531981 scopus 로고
    • Mosaicism in chorionic villus sampling: An analysis of incidence and chromosomes involved in 2612 consecutive cases
    • Wang BB, Rubin CH, Williams Jd (1993) Mosaicism in chorionic villus sampling: an analysis of incidence and chromosomes involved in 2612 consecutive cases. Prenat Diagn 13: 179-90
    • (1993) Prenat Diagn , vol.13 , pp. 179-190
    • Wang, B.B.1    Rubin, C.H.2    Williams, Jd.3
  • 36
    • 0029950129 scopus 로고    scopus 로고
    • Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: Their incidence, likely origins, and mechanisms for all lineage compartmentalizations
    • Wolstenholme J (1996) Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for all lineage compartmentalizations. Prenatal Diag 16:511-524
    • (1996) Prenatal Diag , vol.16 , pp. 511-524
    • Wolstenholme, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.