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Journal Abstract Search

221 related items for PubMed ID: 1433238

  • 21. A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9.
    Wilkinson TA, James RS, Crolla JA, Cockwell AE, Campbell PL, Temple IK.
    Prenat Diagn; 1996 Apr; 16(4):371-4. PubMed ID: 8734817
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  • 23. Trisomy 22 mosaicism limited to skin fibroblasts in a mentally retarded, dysmorphic girl.
    Lund HT, Tranebjaerg L.
    Acta Paediatr Scand; 1990 Apr; 79(6-7):714-8. PubMed ID: 2386070
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  • 24. Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child.
    Röthlisberger B, Zerova T, Kotzot D, Buzhievskaya TI, Balmer D, Schinzel A.
    J Med Genet; 2001 Dec; 38(12):885-8. PubMed ID: 11768396
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  • 26. Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome.
    Flori E, Girodon E, Samama B, Becmeur F, Viville B, Girard-Lemaire F, Doray B, Schluth C, Marcellin L, Boehm N, Goossens M, Pingault V.
    Eur J Hum Genet; 2005 Sep; 13(9):1013-8. PubMed ID: 15915162
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  • 29. Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversion.
    Prasher VP, Roberts E, Norman A, Butler AC, Krishnan VH, McMullan DJ.
    J Med Genet; 1995 Apr; 32(4):306-8. PubMed ID: 7643363
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  • 30. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.
    Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A.
    Am J Med Genet; 1996 Jan 22; 61(3):269-73. PubMed ID: 8741873
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  • 32. Trisomy 18 mosaicism associated with secondary amenorrhea: ratios of mosaicism in different samples and complications.
    Uehara S, Obara Y, Obara T, Funato T, Yaegashi N, Fukaya T, Yajima A.
    Clin Genet; 1996 Feb 22; 49(2):91-4. PubMed ID: 8740920
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  • 36. Trisomy 9 mosaicism in a girl with multiple malformations.
    Diaz-Mares L, Molina B, Carnevale A.
    Ann Genet; 1990 Feb 22; 33(3):165-8. PubMed ID: 2288462
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  • 39. Trisomy 9 mosaicism in two girls with multiple congenital malformations and mental retardation.
    Stoll C, Chognot D, Halb A, Luckel JC.
    J Med Genet; 1993 May 22; 30(5):433-5. PubMed ID: 8320712
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  • 40. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.
    Bocian E, Mazurczak T, Buława E, Stańczak H, Rowicka G.
    J Med Genet; 1993 Jul 22; 30(7):614-5. PubMed ID: 8411041
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