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Volumn 18, Issue 7, 1998, Pages 659-668

Uniparental disomy with and without confined placental mosaicism: A model for trisomic zygote rescue

Author keywords

Confined placental mosaicism; Trisomic zygote rescue; Uniparental disomy

Indexed keywords

DNA;

EID: 0031877890     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199807)18:7<659::AID-PD317>3.0.CO;2-K     Document Type: Article
Times cited : (42)

References (43)
  • 1
    • 0029893780 scopus 로고    scopus 로고
    • The relationship between chromosomal abnormality in the human pre-implantation embryo and development in vitro
    • Almeida, P.A., Bolton, V.N. (1996). The relationship between chromosomal abnormality in the human pre-implantation embryo and development in vitro, Reprod. Fertil. Dev., 8, 235-241.
    • (1996) Reprod. Fertil. Dev. , vol.8 , pp. 235-241
    • Almeida, P.A.1    Bolton, V.N.2
  • 2
    • 0026445152 scopus 로고
    • Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation
    • Bennet, P., Vaughan, J., Henderson, D., Loughna, S., Moore, G. (1992). Association between confined placental trisomy, fetal uniparental disomy, and early intrauterine growth retardation, Lancet, 340, 1284-1285.
    • (1992) Lancet , vol.340 , pp. 1284-1285
    • Bennet, P.1    Vaughan, J.2    Henderson, D.3    Loughna, S.4    Moore, G.5
  • 3
    • 0027180953 scopus 로고
    • Origin of extraembryonic mesoderm in experimental animals: Relevance to chorionic mosaicism in humans
    • Bianchi, D.W., Wilkins-Haug, L.E., Enders, A.C., Hay, E.D. (1993). Origin of extraembryonic mesoderm in experimental animals: relevance to chorionic mosaicism in humans, Am. J. Med. Genet, 33, 542-550.
    • (1993) Am. J. Med. Genet , vol.33 , pp. 542-550
    • Bianchi, D.W.1    Wilkins-Haug, L.E.2    Enders, A.C.3    Hay, E.D.4
  • 5
    • 0025356466 scopus 로고
    • Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15
    • Choo, K.H., Earle, E., Vissel, B., Filby, R.G. (1990). Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15, Genomics, 7, 143-151.
    • (1990) Genomics , vol.7 , pp. 143-151
    • Choo, K.H.1    Earle, E.2    Vissel, B.3    Filby, R.G.4
  • 7
    • 0023840501 scopus 로고
    • An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villi versus fetal tissue
    • Crane, J.P., Cheung, S.W. (1988). An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villi versus fetal tissue, Prenat. Diagn., 8, 119-129.
    • (1988) Prenat. Diagn. , vol.8 , pp. 119-129
    • Crane, J.P.1    Cheung, S.W.2
  • 9
    • 0018939994 scopus 로고
    • A new genetic concept: Uniparental disomy and its potential effect, isodisomy
    • Engel, E. (1980). A new genetic concept: uniparental disomy and its potential effect, isodisomy, Am. J. Med. Genet., 6, 137-143.
    • (1980) Am. J. Med. Genet. , vol.6 , pp. 137-143
    • Engel, E.1
  • 10
    • 0027248861 scopus 로고
    • Uniparental disomy revisited: The first twelve years
    • Engel, E. (1993). Uniparental disomy revisited: the first twelve years, Am. J. Med. Genet., 46, 670-674.
    • (1993) Am. J. Med. Genet. , vol.46 , pp. 670-674
    • Engel, E.1
  • 11
    • 0025773075 scopus 로고
    • Uniparental disomy, isodisomy, and imprinting: Probable effects in man and strategies for their detection
    • Engel, E., DeLozier-Blanchet, C.D. (1991). Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection, Am. J. Med. Genet., 40, 432-439.
    • (1991) Am. J. Med. Genet. , vol.40 , pp. 432-439
    • Engel, E.1    DeLozier-Blanchet, C.D.2
  • 12
    • 0027770784 scopus 로고
    • Identification and characterization of the tuberous sclerosis gene on chromosome 16
    • European Chromosome 16 Tuberous Sclerosis Consortium (1993). Identification and characterization of the tuberous sclerosis gene on chromosome 16, Cell, 75, 1305-1315.
    • (1993) Cell , vol.75 , pp. 1305-1315
  • 13
    • 0023222729 scopus 로고
    • A simple technique for obtaining high quality chromosome preparations from chorionic villus samples using FdU syndronization
    • Gibas, L.M., Grujic, S., Barr, M.A., Jackson, L.G. (1987). A simple technique for obtaining high quality chromosome preparations from chorionic villus samples using FdU syndronization, Prenat. Diagn., 7, 323-327.
    • (1987) Prenat. Diagn. , vol.7 , pp. 323-327
    • Gibas, L.M.1    Grujic, S.2    Barr, M.A.3    Jackson, L.G.4
  • 14
    • 0029077269 scopus 로고
    • Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosiacism 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 mosiacism 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
  • 17
    • 0029117386 scopus 로고
    • Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism
    • Jones, C., Booth, C., Rita, D., Jazmines, L., Spiro, R., McCulloch, B., McCaskill, C., Shaffer, L.G. (1995). Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism, Prenat. Diagn., 15, 843-848.
    • (1995) Prenat. Diagn. , vol.15 , pp. 843-848
    • Jones, C.1    Booth, C.2    Rita, D.3    Jazmines, L.4    Spiro, R.5    McCulloch, B.6    McCaskill, C.7    Shaffer, L.G.8
  • 18
    • 0028676108 scopus 로고
    • Genomic imprinting related to prenatal diagnosis
    • Kalousek, D.K., Barrett, I. (1994). Genomic imprinting related to prenatal diagnosis, Prenat. Diagn., 14, 1191-1201.
    • (1994) Prenat. Diagn. , vol.14 , pp. 1191-1201
    • Kalousek, D.K.1    Barrett, I.2
  • 19
    • 0030055570 scopus 로고    scopus 로고
    • Confined placental mosaicism
    • Kalousek, D.K., Vekemans, M. (1996). Confined placental mosaicism, J. Med. Genet., 33, 529-533.
    • (1996) J. Med. Genet. , vol.33 , pp. 529-533
    • Kalousek, D.K.1    Vekemans, M.2
  • 20
    • 0025991931 scopus 로고
    • Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism
    • Kalousek, D.K., Howard-Peebles, P.N., Olson, S.B., Barrett, I.J., Dorfmann, A., Black, S.H., Schulman, J.D., Wilson, R.D. (1991). Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism, Prenat. Diagn., 11, 743-750.
    • (1991) Prenat. Diagn. , vol.11 , pp. 743-750
    • Kalousek, D.K.1    Howard-Peebles, P.N.2    Olson, S.B.3    Barrett, I.J.4    Dorfmann, A.5    Black, S.H.6    Schulman, J.D.7    Wilson, R.D.8
  • 23
    • 0029832945 scopus 로고    scopus 로고
    • The presence of multinucleated blastomeres in human embryos is correlated with chromosomal abnormalities
    • Kligman, I., Benadiva, C., Alikani, M., Munné, S. (1996). The presence of multinucleated blastomeres in human embryos is correlated with chromosomal abnormalities, Hum. Reprod., 11, 1492-1498.
    • (1996) Hum. Reprod. , vol.11 , pp. 1492-1498
    • Kligman, I.1    Benadiva, C.2    Alikani, M.3    Munné, S.4
  • 24
    • 0028867372 scopus 로고
    • Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7
    • Langlois, S., Yong, S.L., Wilson, R.D., Kwong, L.C., Kalousek, D.K. (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
  • 25
    • 0029162269 scopus 로고
    • Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
    • Ledbetter, D.H., 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
  • 29
    • 0021357181 scopus 로고
    • The origin of mosaic Down syndrome: Four cases with chromosome markers
    • Niikkawa, N., Kajii, T. (1984). The origin of mosaic Down syndrome: four cases with chromosome markers, Am. J. Hum. Genet., 36, 123-130.
    • (1984) Am. J. Hum. Genet. , vol.36 , pp. 123-130
    • Niikkawa, N.1    Kajii, T.2
  • 32
    • 0028854976 scopus 로고
    • Molecular studies of chromosomal mosaicism: Relative frequency of chromosome gain or loss and possible role of cell selection
    • Robinson, W.P., Binkert, F., Bernasconi, F., Lorda-Sanchez, I., Werder, E.A., Schinzel, A.A. (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
    • 0028094977 scopus 로고
    • Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosiac 46,XX/ 47,XX,+14 karyotype
    • Sirchia, S.M., De Andreis, C., Pariani, S., Grimoldi, M.G., Molinari, A., Buscaglia, M., Simoni, G. (1994). Chromosome 14 maternal uniparental disomy in the euploid cell line of a fetus with mosiac 46,XX/ 47,XX,+14 karyotype, Hum. Genet., 94, 355-358.
    • (1994) Hum. Genet. , vol.94 , pp. 355-358
    • Sirchia, S.M.1    De Andreis, C.2    Pariani, S.3    Grimoldi, M.G.4    Molinari, A.5    Buscaglia, M.6    Simoni, G.7
  • 34
    • 0026474734 scopus 로고
    • Human embryo biopsy on the 2nd day after insemination for preimplantation diagnosis: Removal of a quarter of embryo retards cleavage
    • Tarin, J.J., Conaghan, J., Winston, R.M.L., Handyside, A.H. (1992). Human embryo biopsy on the 2nd day after insemination for preimplantation diagnosis: removal of a quarter of embryo retards cleavage, Fertil. Steril., 5, 970-976.
    • (1992) Fertil. Steril. , vol.5 , pp. 970-976
    • Tarin, J.J.1    Conaghan, J.2    Winston, R.M.L.3    Handyside, A.H.4
  • 36
    • 0028798660 scopus 로고
    • Retrospective study of trisomy 18 in chorionic villi with fluorescent in situ hybridization on archival direct preparations
    • Van Opstal, D., Van den Berg, C., Jahoda, M.G.J., Brandenburg, H., Los, F.J., In 't Veld, P.A. (1995). Retrospective study of trisomy 18 in chorionic villi with fluorescent in situ hybridization on archival direct preparations, Prenat. Diagn., 15, 51-55.
    • (1995) Prenat. Diagn. , vol.15 , pp. 51-55
    • Van Opstal, D.1    Van Den Berg, C.2    Jahoda, M.G.J.3    Brandenburg, H.4    Los, F.J.5    In 't Veld, P.A.6
  • 41
    • 0029797559 scopus 로고    scopus 로고
    • Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation
    • Webb, A.L., Sturgiss, S., Warwicker, P., Robson, S.C., Goodship, J.A., Wolstenholme, J. (1996). Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation, Prenat. Diagn., 16, 958-962.
    • (1996) Prenat. Diagn. , vol.16 , pp. 958-962
    • Webb, A.L.1    Sturgiss, S.2    Warwicker, P.3    Robson, S.C.4    Goodship, J.A.5    Wolstenholme, J.6
  • 42
    • 0029886674 scopus 로고    scopus 로고
    • A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9
    • Wilkinson, T.A., James, R.S., Crolla, J.A., Cockwell, A.E., Campbell, P.L., Temple, I.K. (1996). A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9, Prenat. Diagn., 16, 371-374.
    • (1996) Prenat. Diagn. , vol.16 , pp. 371-374
    • Wilkinson, T.A.1    James, R.S.2    Crolla, J.A.3    Cockwell, A.E.4    Campbell, P.L.5    Temple, I.K.6
  • 43
    • 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 cell lineage compartmentalization
    • Wolstenholme, J. (1996). Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16 and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization, Prenat. Diagn., 16, 511-524.
    • (1996) Prenat. Diagn. , vol.16 , pp. 511-524
    • Wolstenholme, J.1


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