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Prenatal Diagnosis
Volumn 25, Issue 11, 2005, Pages 1067-1069
Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis [7]
Author keywords

[No Author keywords available]
Indexed keywords

AMNIOCENTESIS; AMNION CELL; AUTOPSY; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME ANALYSIS; DNA ISOLATION; FEMALE; FETUS; FETUS KARYOTYPING; GESTATION PERIOD; HUMAN; LETTER; POLYMERASE CHAIN REACTION; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SHORT TANDEM REPEAT; TRISOMY 7;
EID: 28544436461     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1297     Document Type: Letter
Times cited : (13)
References (8)
  • 1
    • 0042320922 scopus 로고    scopus 로고
    • Prenatal diagnosis of a trisomy 7/maternal uniparental heterodisomy 7 mosaic fetus
    • Bilimoria KY, Rothenberg JM. 2003. Prenatal diagnosis of a trisomy 7/maternal uniparental heterodisomy 7 mosaic fetus. Am J Med Genet 118A: 60-63.
    • (2003) Am J Med Genet , vol.118 A , pp. 60-63
    • Bilimoria, K.Y.1    Rothenberg, J.M.2
  • 2
    • 0030973681 scopus 로고    scopus 로고
    • Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20 and 21: Karyotype/phenotype correlations
    • Hsu LYF, Yu M-T, Neu RL, et al. 1997. Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20 and 21: karyotype/phenotype correlations. Prenat Diagn 17: 201-242.
    • (1997) Prenat Diagn , vol.17 , pp. 201-242
    • Hsu, L.Y.F.1    Yu, M.-T.2    Neu, R.L.3
  • 3
    • 0027203993 scopus 로고
    • Hypomelanosis of Ito associated with mosaicism for trisomy 7 and apparent 'pseudomosaicism' at amniocentesis
    • Jenkins D, Martin K, Young ID. 1993. Hypomelanosis of Ito associated with mosaicism for trisomy 7 and apparent 'pseudomosaicism' at amniocentesis. J Med Genet 30: 783-784.
    • (1993) J Med Genet , vol.30 , pp. 783-784
    • Jenkins, D.1    Martin, K.2    Young, I.D.3
  • 4
    • 0035990103 scopus 로고    scopus 로고
    • Prenatally detected trisomy 7 mosaicism in a dysmorphic child
    • Kivirikko S, Salonen R, Salo A, von Koskull H. 2002. Prenatally detected trisomy 7 mosaicism in a dysmorphic child. Prenat Diagn 22: 541-544.
    • (2002) Prenat Diagn , vol.22 , pp. 541-544
    • Kivirikko, S.1    Salonen, R.2    Salo, A.3    Von Koskull, H.4
  • 5
    • 0034113750 scopus 로고    scopus 로고
    • Maternal uniparental disomy 7-review and further delineation of the phenotype
    • Kotzot D, Balmer D, Baumer A, et al. 2000. Maternal uniparental disomy 7-review and further delineation of the phenotype. Eur J Pediatr 159: 247-256.
    • (2000) Eur J Pediatr , vol.159 , pp. 247-256
    • Kotzot, D.1    Balmer, D.2    Baumer, A.3
  • 6
    • 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
  • 7
    • 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
  • 8
    • 0036933177 scopus 로고    scopus 로고
    • Trisomy 7 mosaicism: Prognosis after prenatal diagnosis
    • Warburton D. 2002. Trisomy 7 mosaicism: prognosis after prenatal diagnosis. Prenat Diagn 22: 1239-1240.
    • (2002) Prenat Diagn , vol.22 , pp. 1239-1240
    • Warburton, D.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.