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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

147 related items for PubMed ID: 9516010

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  • 4. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G, Novotna D, Simandlova M, Havlovicova M, Zumrová A, Kocarek E, Sedlacek Z.
    Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
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  • 6. Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15.
    Cotter PD, Ledesma CT, Dietz LG, Pusso S, Wohlferd MM, Goldberg JD.
    Prenat Diagn; 1999 Aug; 19(8):721-6. PubMed ID: 10451515
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  • 9. Detection of translocations involving the Y-chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH.
    Verlinsky Y, Ginsberg N, Chmura M, White M, Strom C, Kuliev A.
    Prenat Diagn; 1998 Apr; 18(4):390-2. PubMed ID: 9602488
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  • 10. Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.
    Freeman SB, May KM, Pettay D, Fernhoff PM, Hassold TJ.
    Am J Med Genet; 1993 Mar 01; 45(5):625-30. PubMed ID: 8456836
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  • 14. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
    Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brøndum-Nielsen K.
    Prenat Diagn; 1997 Apr 01; 17(4):369-74. PubMed ID: 9160390
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  • 15. Prenatally detected paternal uniparental chromosome 13 isodisomy.
    Järvelä I, Savukoski M, Ammälä P, von Koskull H.
    Prenat Diagn; 1998 Nov 01; 18(11):1169-73. PubMed ID: 9854727
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  • 19. Relevance to prenatal diagnosis of the identification of a human Y/autosome translocation by Y-chromosome-specific in situ hybridisation.
    Ellis PM, West JD, West KM, Murray RS, Coyle MC.
    Mol Reprod Dev; 1990 Jan 01; 25(1):37-41. PubMed ID: 2393582
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  • 20. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A, Lapunzina P, Palomares M, Molina MA, Galán E, López Pajares I.
    Eur J Med Genet; 2005 Jan 01; 48(2):159-66. PubMed ID: 16053907
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