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PUBMED FOR HANDHELDS

Journal Abstract Search

188 related items for PubMed ID: 26137780

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  • 30. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
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  • 35. Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21.
    Lee C, Fowler DJ, Lemyre E, Sandstrom MM, Holmes LB, Morton CC.
    Am J Med Genet; 2001 May 01; 100(3):246-50. PubMed ID: 11343311
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  • 36. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
    Frints SG, Moerman P, Fryns JP.
    Genet Couns; 1996 May 01; 7(4):313-9. PubMed ID: 8985736
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  • 39. Prenatal diagnosis of trisomy 2 mosaicism: a case report.
    Sifakis S, Velissariou V, Papadopoulou E, Petersen MB, Koumantakis E.
    Fetal Diagn Ther; 2004 May 01; 19(6):488-90. PubMed ID: 15539872
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  • 40. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
    Shaffer LG, Spikes AS, Macha M, Dunn R.
    J Reprod Med; 1996 May 01; 41(5):367-71. PubMed ID: 8725766
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