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Volumn 42, Issue 5, 2002, Pages 486-489

Prenatal diagnosis of mosaic trisomy 20 in New Zealand

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CHORION VILLUS SAMPLING; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DATA BASE; FEMALE; FOLLOW UP; HUMAN; INCIDENCE; KARYOTYPE; LABORATORY; MEDICAL RECORD; MOSAICISM; NEW ZEALAND; PARENT COUNSELING; PHENOTYPE; PREDICTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RELIABILITY; RETROSPECTIVE STUDY; RISK; TRISOMY;

EID: 0036853699     PISSN: 00048666     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0004-8666.2002.00486.x     Document Type: Article
Times cited : (11)

References (18)
  • 1
    • 0025753402 scopus 로고
    • A revisit of trisomy 20 mosaicism in prenatal diagnosis - An overview of 103 cases
    • Jan
    • Hsu LY, Kaffe S, Perlis TE. A revisit of trisomy 20 mosaicism in prenatal diagnosis - an overview of 103 cases. Prenat Diagn. 1991 Jan; 11 (1): 7-15.
    • (1991) Prenat. Diagn. , vol.11 , Issue.1 , pp. 7-15
    • Hsu, L.Y.1    Kaffe, S.2    Perlis, T.E.3
  • 2
    • 0035869116 scopus 로고    scopus 로고
    • Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development
    • Mar 15
    • Baty BJ, Olson SB, Magenis RE, Carey JC. Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development. Am J Med Genet. 2001 Mar 15; 99 (3): 210-216.
    • (2001) Am. J. Med. Genet. , vol.99 , Issue.3 , pp. 210-216
    • Baty, B.J.1    Olson, S.B.2    Magenis, R.E.3    Carey, J.C.4
  • 3
    • 0032574683 scopus 로고    scopus 로고
    • Dilemma of trisomy 20 mosaicism detected prenatally: Is it an innocent finding?
    • Apr 28
    • Reish O, Wolach B, Amiel A, Kedar I, Dolfin T, Fejgin M. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding? Am J Med Genet. 1998 Apr 28; 77 (1): 72-75.
    • (1998) Am. J. Med. Genet. , vol.77 , Issue.1 , pp. 72-75
    • Reish, O.1    Wolach, B.2    Amiel, A.3    Kedar, I.4    Dolfin, T.5    Fejgin, M.6
  • 4
    • 0022628642 scopus 로고
    • Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20 mosaicism
    • Apr
    • Holzgreve W, Golabi M, Bradley J. Multiple congenital anomalies in a child born after prenatal diagnosis of trisomy 20 mosaicism. Clin Genet. 1986 Apr; 29 (4): 342-344.
    • (1986) Clin. Genet. , vol.29 , Issue.4 , pp. 342-344
    • Holzgreve, W.1    Golabi, M.2    Bradley, J.3
  • 5
    • 0023429133 scopus 로고
    • Trisomy 20 mosaicism in prenatal diagnosis - A review and update
    • Oct
    • Hsu LY, Kaffe S, Perlis TE. Trisomy 20 mosaicism in prenatal diagnosis - a review and update. Prenat Diagn. 1987 Oct; 7 (8): 581-596.
    • (1987) Prenat. Diagn. , vol.7 , Issue.8 , pp. 581-596
    • Hsu, L.Y.1    Kaffe, S.2    Perlis, T.E.3
  • 7
    • 0029848904 scopus 로고    scopus 로고
    • Cytogenetic and molecular genetic characterisation of trisomy 20 mosaicism in fetal blood and tissues
    • Oct
    • Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S. Cytogenetic and molecular genetic characterisation. of trisomy 20 mosaicism in fetal blood and tissues. Prenat Diagn. 1996 Oct; 16 (10): 893-897.
    • (1996) Prenat. Diagn. , vol.16 , Issue.10 , pp. 893-897
    • Micale, M.A.1    Wolff, D.J.2    Dickerman, L.H.3    Redline, R.4    Conroy, J.M.5    Schwartz, S.6
  • 9
    • 0023338943 scopus 로고
    • Prenatal diagnosis of trisomy 20 mosaicism indicating an extraembryonic origin
    • May
    • Baldinger S, Millard C, Schmeling D, Bendel RP. Prenatal diagnosis of trisomy 20 mosaicism indicating an extraembryonic origin. Prenat Diagn. 1987 May; 7 (4): 273-276.
    • (1987) Prenat. Diagn. , vol.7 , Issue.4 , pp. 273-276
    • Baldinger, S.1    Millard, C.2    Schmeling, D.3    Bendel, R.P.4
  • 10
    • 0024547811 scopus 로고
    • Chromosome analyses from urinary sediment: Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism
    • Mar 23
    • Miny P, Karabacak Z, Hammer P, Schulte-Vellentin M, Holzgreve W. Chromosome analyses from urinary sediment: postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism. N Eng J Med. 1989 Mar 23; 320 (12): 809.
    • (1989) N. Eng. J. Med. , vol.320 , Issue.12 , pp. 809
    • Miny, P.1    Karabacak, Z.2    Hammer, P.3    Schulte-Vellentin, M.4    Holzgreve, W.5
  • 11
    • 0035105118 scopus 로고    scopus 로고
    • Identification of interstitial uniparental disomy (UPD) (14) and complete maternal UPD (20) in a cohort of growth retarded patients
    • Feb
    • Eggermann T, Mergenthaler S, Eggermann K, Albers A, Linnemann K, Fusch C, Ranke MB, Wollmann HA. Identification of interstitial uniparental disomy (UPD) (14) and complete maternal UPD (20) in a cohort of growth retarded patients. J Med Genet. 2001 Feb; 38 (2): 86-89.
    • (2001) J. Med. Genet. , vol.38 , Issue.2 , pp. 86-89
    • Eggermann, T.1    Mergenthaler, S.2    Eggermann, K.3    Albers, A.4    Linnemann, K.5    Fusch, C.6    Ranke, M.B.7    Wollmann, H.A.8
  • 13
    • 0032433682 scopus 로고    scopus 로고
    • Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins
    • Dec 22
    • Hayward BE, Moran V, Strain L, Bonthron DT. Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins. Proc Natl Acad Sci USA. 1998 Dec 22; 95 (26): 15475-15480.
    • (1998) Proc. Natl. Acad. Sci. USA. , vol.95 , Issue.26 , pp. 15475-15480
    • Hayward, B.E.1    Moran, V.2    Strain, L.3    Bonthron, D.T.4
  • 14
    • 0026642901 scopus 로고
    • Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male
    • Jul
    • Brotham AR, Rehberg K, Storto PD, Phillps SE, Mosby RT. Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male. Clin Genet. 1992 Jul; 42 (1): 47-49.
    • (1992) Clin. Genet. , vol.42 , Issue.1 , pp. 47-49
    • Brotham, A.R.1    Rehberg, K.2    Storto, P.D.3    Phillps, S.E.4    Mosby, R.T.5
  • 15
    • 0028934283 scopus 로고
    • An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line
    • Feb
    • Batista DA, Escallon C, Blakemore KJ, Stetten G. An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line. Prenat Diagn. 1995 Feb; 15 (2): 123-127.
    • (1995) Prenat. Diagn. , vol.15 , Issue.2 , pp. 123-127
    • Batista, D.A.1    Escallon, C.2    Blakemore, K.J.3    Stetten, G.4
  • 16
    • 0026865925 scopus 로고
    • Non-mosaic trisomy 20 in cultures of amniotic fluid from a fetus with serious congenital malformation
    • May
    • Hsieh CC, Hsu JJ, Lo LM, Hsieh TT, Soong YK. Non-mosaic trisomy 20 in cultures of amniotic fluid from a fetus with serious congenital malformation. J Formos Med Assoc. 1992 May; 91 (5): 543-544.
    • (1992) J. Formos. Med. Assoc. , vol.91 , Issue.5 , pp. 543-544
    • Hsieh, C.C.1    Hsu, J.J.2    Lo, L.M.3    Hsieh, T.T.4    Soong, Y.K.5
  • 17
    • 0024541823 scopus 로고
    • Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus
    • Apr
    • Myers TL, Prouty LA. Non-mosaic trisomy 20 in amniotic fluid cultures with minor anomalies in the fetus. Clin Genet. 1989 Apr; 35 (4): 233-236.
    • (1989) Clin. Genet. , vol.35 , Issue.4 , pp. 233-236
    • Myers, T.L.1    Prouty, L.A.2


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