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Journal Abstract Search

127 related items for PubMed ID: 9564560

  • 1. Molecular genetic analysis of the Prader-Willi syndrome by using fluorescent multiplex PCR of the dinucleotide repeats on chromosome 15q11-q13.
    Lee MJ, Nishio H, Nagai T, Okamoto N, Yuki T, Sumino K.
    Clin Chim Acta; 1998 Mar 09; 271(1):89-96. PubMed ID: 9564560
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  • 2. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP.
    Genet Couns; 1999 Mar 09; 10(2):123-32. PubMed ID: 10422004
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  • 3. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L, Chamberlain SJ.
    Pediatr Clin North Am; 2015 Jun 09; 62(3):587-606. PubMed ID: 26022164
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  • 4. Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region.
    Butler MG, Bittel D, Talebizadeh Z.
    J Med Genet; 2002 Mar 09; 39(3):202-4. PubMed ID: 11897825
    [No Abstract] [Full Text] [Related]

  • 5. [Molecular analysis in Prader-Willi syndrome diagnosis].
    Szpecht-Potocka A.
    Med Wieku Rozwoj; 1999 Mar 09; 3(3):407-19. PubMed ID: 10910667
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  • 6. Approaches to the prenatal diagnosis of the Prader-Willi syndrome.
    Schinzel A.
    Hum Genet; 1986 Nov 09; 74(3):327. PubMed ID: 3781563
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  • 7. [The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome].
    Iourov IY, Vorsanova SG, Kurinnaaya OS, Kolotii AD, Demidova IA, Kravets VS, Yurov YB.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2014 Nov 09; 114(1):49-53. PubMed ID: 24637817
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  • 8. [Prader-Willi-Labhart syndrome: relations with the hypothalamus and chromosome 15].
    Touraine P, Mbikay M, Seidah NG, Chrétien M.
    Ann Endocrinol (Paris); 1990 Nov 09; 51(5-6):202-8. PubMed ID: 2130760
    [Abstract] [Full Text] [Related]

  • 9. Genetic testing for Prader-Willi and Angelman syndromes.
    Schad CR, Jalal SM, Thibodeau SN.
    Mayo Clin Proc; 1995 Dec 09; 70(12):1195-6. PubMed ID: 7490922
    [No Abstract] [Full Text] [Related]

  • 10. Molecular screening for proximal 15q abnormalities in a mentally retarded population.
    Jacobsen J, King BH, Leventhal BL, Christian SL, Ledbetter DH, Cook EH.
    J Med Genet; 1998 Jul 09; 35(7):534-8. PubMed ID: 9678696
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  • 13. [Unbalanced translocation t (5;15) in a patient with Prader-Willi syndrome].
    Bai JL, Wang H, Yang YL, Song F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec 09; 27(6):664-7. PubMed ID: 21154328
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  • 18. Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome.
    Ninomiya S, Yokoyama Y, Kawakami M, Une T, Maruyama H, Morishima T.
    Pediatr Int; 2005 Oct 09; 47(5):541-5. PubMed ID: 16190961
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  • 19. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
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