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Journal Abstract Search

379 related items for PubMed ID: 8741873

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  • 3. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism.
    Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, Resta RG, Surti U, Suslak L, Verp MS, Ledbetter DH.
    Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806
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  • 8. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
    Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B.
    Eur J Hum Genet; 1997 Apr; 5(5):308-14. PubMed ID: 9412788
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  • 11. 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.
    Am J Med Genet; 1995 Aug 28; 58(2):147-51. PubMed ID: 8533806
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  • 14. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
    Chen CP, Lin HM, Su YN, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep 28; 49(3):341-50. PubMed ID: 21056321
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  • 20. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
    Turleau C, Rethoré MO, Junien C, Lejeune J, de Grouchy J.
    Ann Genet; 1979 Sep 28; 22(3):178-81. PubMed ID: 316677
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