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Journal Abstract Search

338 related items for PubMed ID: 3688019

  • 1. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
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  • 2. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
    Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH.
    Am J Med Genet; 1987 Dec; 28(4):791-802. PubMed ID: 3688017
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  • 3. 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; 20(2):255-63. PubMed ID: 2858158
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  • 4. Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.
    Hamabe J, Fukushima Y, Harada N, Abe K, Matsuo N, Nagai T, Yoshioka A, Tonoki H, Tsukino R, Niikawa N.
    Am J Med Genet; 1991 Oct 01; 41(1):54-63. PubMed ID: 1683159
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  • 5. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
    Gregory CA, Kirkilionis AJ, Greenberg CR, Chudley AE, Hamerton JL.
    Am J Med Genet; 1990 Apr 01; 35(4):536-45. PubMed ID: 1970703
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  • 7. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
    Varela MC, Lopes GM, Koiffmann CP.
    Ann Genet; 2004 Apr 01; 47(3):267-73. PubMed ID: 15337472
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  • 8. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
    Nicholls RD, Knoll JH, Glatt K, Hersh JH, Brewster TD, Graham JM, Wurster-Hill D, Wharton R, Latt SA.
    Am J Med Genet; 1989 May 01; 33(1):66-77. PubMed ID: 2568752
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  • 12. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA.
    Clin Genet; 2004 Jun 01; 65(6):477-82. PubMed ID: 15151506
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  • 15. Deletion of small nuclear ribonucleoprotein polypeptide N (SNRPN) in Prader-Willi syndrome detected by fluorescence in situ hybridization: two sibs with the typical phenotype without a cytogenetic deletion in chromosome 15q.
    Ishikawa T, Kibe T, Wada Y.
    Am J Med Genet; 1996 Apr 24; 62(4):350-2. PubMed ID: 8723064
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  • 20. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
    Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S.
    Am J Med Genet; 1997 Feb 11; 68(4):433-40. PubMed ID: 9021017
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