메뉴 건너뛰기




Volumn 75, Issue 3, 2004, Pages 376-385

Trisomy recurrence: A reconsideration based on North American data

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; FEMALE; HUMAN; KARYOTYPE; KARYOTYPE 47,XXX; KARYOTYPE 47,XXY; MATERNAL AGE; MORBIDITY; NORTH AMERICA; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECURRENCE RISK; SPONTANEOUS ABORTION; TRISOMY; TRISOMY 13; TRISOMY 18; TRISOMY 21;

EID: 4143106805     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/423331     Document Type: Article
Times cited : (132)

References (26)
  • 1
    • 0035691962 scopus 로고    scopus 로고
    • Familial Down syndrome: Evidence supporting cytoplasmic inheritance
    • Arbuzova S, Cuckle H, Mueller R, Sehni I (2001) Familial Down syndrome: evidence supporting cytoplasmic inheritance. Clin Genet 60:456-462
    • (2001) Clin Genet , vol.60 , pp. 456-462
    • Arbuzova, S.1    Cuckle, H.2    Mueller, R.3    Sehni, I.4
  • 2
    • 0036854457 scopus 로고    scopus 로고
    • Meiotic cohesion requires accumulation of ORD on chromosomes before condensation
    • Balicky EM, Endres MW, Lai C, Bickel SE (2002) Meiotic cohesion requires accumulation of ORD on chromosomes before condensation. Mol Biol Cell 11:3890-3900
    • (2002) Mol Biol Cell , vol.11 , pp. 3890-3900
    • Balicky, E.M.1    Endres, M.W.2    Lai, C.3    Bickel, S.E.4
  • 3
    • 0037318792 scopus 로고    scopus 로고
    • Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies
    • Beever CL, Stephenson MD, Peñaherrera MS, Jiang RH, Kalousek DK, Hayden M, Field L, Brown CJ, Robinson WP (2003) Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies. Am J Hum Genet 72:399-407
    • (2003) Am J Hum Genet , vol.72 , pp. 399-407
    • Beever, C.L.1    Stephenson, M.D.2    Peñaherrera, M.S.3    Jiang, R.H.4    Kalousek, D.K.5    Hayden, M.6    Field, L.7    Brown, C.J.8    Robinson, W.P.9
  • 4
    • 0343384391 scopus 로고    scopus 로고
    • Genome-wide variation in recombination in female meiosis: A risk factor for non-disjunction of chromosome 21
    • Brown AS, Feingold E, Broman KW, Sherman SL (2000) Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21. Hum Mol Genet 9:515-523
    • (2000) Hum Mol Genet , vol.9 , pp. 515-523
    • Brown, A.S.1    Feingold, E.2    Broman, K.W.3    Sherman, S.L.4
  • 5
    • 0034605363 scopus 로고    scopus 로고
    • Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line
    • Bruyere H, Rupps R, Kuchinka BD, Friedman JM, Robinson WP (2000) Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line. Am J Med Genet 94:35-41
    • (2000) Am J Med Genet , vol.94 , pp. 35-41
    • Bruyere, H.1    Rupps, R.2    Kuchinka, B.D.3    Friedman, J.M.4    Robinson, W.P.5
  • 6
    • 0033555450 scopus 로고    scopus 로고
    • Frequencies of chromosomal abnormalities at amniocentesis over 20 years of cytogenetic analyses in one laboratory
    • Caron L, Tihy F, Dallaire L (1999) Frequencies of chromosomal abnormalities at amniocentesis over 20 years of cytogenetic analyses in one laboratory. Am J Med Genet 82:149-159
    • (1999) Am J Med Genet , vol.82 , pp. 149-159
    • Caron, L.1    Tihy, F.2    Dallaire, L.3
  • 8
    • 0035319804 scopus 로고    scopus 로고
    • To err (meiotically) is human: The genesis of human aneuploidy
    • Hassold T, Hunt P (2001) To err (meiotically) is human: the genesis of human aneuploidy. Nat Rev Genet 2:280-291
    • (2001) Nat Rev Genet , vol.2 , pp. 280-291
    • Hassold, T.1    Hunt, P.2
  • 9
    • 0036099484 scopus 로고    scopus 로고
    • Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation
    • Hodges CA, Ilagan A, Jennings D, Keri R, Nilson J, Hunt PA (2002) Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation. Hum Reprod 17: 1171-1180
    • (2002) Hum Reprod , vol.17 , pp. 1171-1180
    • Hodges, C.A.1    Ilagan, A.2    Jennings, D.3    Keri, R.4    Nilson, J.5    Hunt, P.A.6
  • 10
    • 0002682681 scopus 로고
    • Chromosome anomalies: Prevalence, risks, and recurrence
    • Brock DJH, Rodeck CH, Ferguson-Smith MA (eds). Churchill Livingstone, Edinburgh
    • Hook EB (1992) Chromosome anomalies: prevalence, risks, and recurrence. In: Brock DJH, Rodeck CH, Ferguson-Smith MA (eds) Prenatal diagnosis and screening. Churchill Livingstone, Edinburgh
    • (1992) Prenatal Diagnosis and Screening
    • Hook, E.B.1
  • 13
    • 0031869212 scopus 로고    scopus 로고
    • Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnancies
    • James RS, Ellis K, Pettay D, Jacobs PA (1998) Cytogenetic and molecular study of four couples with multiple trisomy 21 pregnancies. Eur J Hum Genet 6:207-212
    • (1998) Eur J Hum Genet , vol.6 , pp. 207-212
    • James, R.S.1    Ellis, K.2    Pettay, D.3    Jacobs, P.A.4
  • 16
    • 0033023149 scopus 로고    scopus 로고
    • Fetal loss in Down syndrome pregnancies
    • Morris JK, Wald NJ, Watt HC (1999) Fetal loss in Down syndrome pregnancies. Prenat Diagn 19:142-145
    • (1999) Prenat Diagn , vol.19 , pp. 142-145
    • Morris, J.K.1    Wald, N.J.2    Watt, H.C.3
  • 22
    • 0034810253 scopus 로고    scopus 로고
    • What is the true fetal loss in pregnancies affected by trisomy 21 and how does this influence whether first trimester detection rates are superior to those in the second trimester?
    • Spencer K (2001) What is the true fetal loss in pregnancies affected by trisomy 21 and how does this influence whether first trimester detection rates are superior to those in the second trimester? Prenat Diagn 21:788-789
    • (2001) Prenat Diagn , vol.21 , pp. 788-789
    • Spencer, K.1
  • 23
    • 0021210651 scopus 로고
    • Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration
    • Stene J, Stene E, Mikkelsen M (1984) Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. Prenat Diagn 4:81-95
    • (1984) Prenat Diagn , vol.4 , pp. 81-95
    • Stene, J.1    Stene, E.2    Mikkelsen, M.3
  • 24
    • 0022415610 scopus 로고
    • Trisomy 21 Down syndrome: Parental mosaicism
    • Uchida IA, Freeman VC (1985) Trisomy 21 Down syndrome: parental mosaicism. Hum Genet 70:246-248
    • (1985) Hum Genet , vol.70 , pp. 246-248
    • Uchida, I.A.1    Freeman, V.C.2
  • 25
    • 0023603302 scopus 로고
    • Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions
    • Warburton D, Kline J, Stein Z, Hutzler M, Chin A, Hassold T (1987) Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions. Am J Hum Genet 41:465-483
    • (1987) Am J Hum Genet , vol.41 , pp. 465-483
    • Warburton, D.1    Kline, J.2    Stein, Z.3    Hutzler, M.4    Chin, A.5    Hassold, T.6
  • 26
    • 0344289522 scopus 로고    scopus 로고
    • Genetic variation in rates of nondisjunction: Association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster
    • Zwick ME, Salstrom JL, Langley CH (1999) Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster. Genetics 152:1605-1614
    • (1999) Genetics , vol.152 , pp. 1605-1614
    • Zwick, M.E.1    Salstrom, J.L.2    Langley, C.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.