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Journal Abstract Search

155 related items for PubMed ID: 8222009

  • 1. [High-resolution cytogenetic study of a patient with Prader-Willi syndrome].
    Shi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Jun; 15(3):217-20. PubMed ID: 8222009
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  • 2. High-resolution cytogenetic studies in patients with Prader-Willi syndrome.
    Takano T, Nakagome Y, Nagafuchi S, Tanaka F, Nakamura Y, Nagano T, Tanae A, Hibi I.
    Clin Genet; 1986 Oct; 30(4):241-8. PubMed ID: 3791673
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  • 3. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
    Delach JA, Rosengren SS, Kaplan L, Greenstein RM, Cassidy SB, Benn PA.
    Am J Med Genet; 1994 Aug 01; 52(1):85-91. PubMed ID: 7977469
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  • 4. [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Götz J, Krüger G, Westphal BC, Pelz L.
    Kinderarztl Prax; 1989 May 01; 57(5):239-43. PubMed ID: 2747122
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  • 5. Interstitial 15q deletion without a classic Prader-Willi phenotype.
    Galán F, Aguilar MS, González J, Clemente F, Sánchez R, Tapia M, Moya M.
    Am J Med Genet; 1991 Mar 15; 38(4):532-4. PubMed ID: 2063892
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  • 6. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
    Magenis RE, Toth-Fejel S, Allen LJ, Black M, Brown MG, Budden S, Cohen R, Friedman JM, Kalousek D, Zonana J.
    Am J Med Genet; 1990 Mar 15; 35(3):333-49. PubMed ID: 2309780
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  • 7. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
    Cassidy SB, Thuline HC, Holm VA.
    Am J Med Genet; 1984 Feb 15; 17(2):485-95. PubMed ID: 6336316
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  • 12. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G, Tükün A, Yalaz K, Bökesoy I.
    Turk J Pediatr; 1993 Feb 15; 35(4):333-6. PubMed ID: 8160287
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  • 14. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
    Puvabanditsin S, Garrow E, Razi S, Mohar AG, Tadros JJ, Phattraprayoon N, Patel P.
    Genet Couns; 2007 Feb 15; 18(4):417-21. PubMed ID: 18286823
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  • 15. Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi syndrome.
    Hoo JJ, Chao MC, Samuel IP, Morgan AM.
    Clin Genet; 1990 Mar 15; 37(3):161-6. PubMed ID: 2323086
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  • 16. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec 15; 28(4):813-20. PubMed ID: 3688019
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  • 18. Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
    Schwartz S, Max SR, Panny SR, Cohen MM.
    Am J Med Genet; 1985 Feb 15; 20(2):255-63. PubMed ID: 2858158
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