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Journal Abstract Search

353 related items for PubMed ID: 7649555

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  • 2. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
    Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG.
    Eur J Hum Genet; 2007 Apr; 15(4):432-40. PubMed ID: 17264869
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  • 4. FISH analysis in Prader-Willi and Angelman syndrome patients.
    Bettio D, Rizzi N, Giardino D, Grugni G, Briscioli V, Selicorni A, Carnevale F, Larizza L.
    Am J Med Genet; 1995 Mar 27; 56(2):224-8. PubMed ID: 7625450
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  • 6. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
    Kuwano A, Mutirangura A, Dittrich B, Buiting K, Horsthemke B, Saitoh S, Niikawa N, Ledbetter SA, Greenberg F, Chinault AC.
    Hum Mol Genet; 1992 Sep 27; 1(6):417-25. PubMed ID: 1363801
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  • 7. FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.
    Teshima I, Chadwick D, Chitayat D, Kobayashi J, Ray P, Shuman C, Siegel-Bartelt J, Strasberg P, Weksberg R.
    Am J Med Genet; 1996 Mar 29; 62(3):217-23. PubMed ID: 8882776
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  • 8. 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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  • 9. Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.
    Smith A, Prasad M, Deng ZM, Robson L, Woodage T, Trent RJ.
    Arch Dis Child; 1995 May 01; 72(5):397-402. PubMed ID: 7618904
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  • 14. Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.
    Horsthemke B, Maat-Kievit A, Sleegers E, van den Ouweland A, Buiting K, Lich C, Mollevanger P, Beverstock G, Gillessen-Kaesbach G, Schwanitz G.
    J Med Genet; 1996 Oct 01; 33(10):848-51. PubMed ID: 8933339
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  • 15. Unbalanced translocation t(15;22) in "severe" Prader-Willi syndrome.
    Smith A, Jauch A, St Heaps L, Robson L, Kearney B.
    Ann Genet; 2000 Oct 01; 43(3-4):125-30. PubMed ID: 11164193
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  • 17. The human genome: detecting chromosomal deletions: Angelman and Prader-Willi syndromes.
    Morris-Rosendahl DJ, Back E.
    Am J Psychiatry; 2002 Mar 01; 159(3):372. PubMed ID: 11869997
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  • 18. Detection of chromosome 15 deletion in Prader-Willi syndrome using fluorescence in situ hybridization.
    Suzuki Y, Sasagawa I, Yazawa H, Tateno T, Nakada T.
    Arch Androl; 2000 Mar 01; 45(1):13-7. PubMed ID: 10959497
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