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Journal Abstract Search

131 related items for PubMed ID: 1684091

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  • 4. 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; 35(4):536-45. PubMed ID: 1970703
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  • 5. 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; 35(3):333-49. PubMed ID: 2309780
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  • 6. 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; 33(1):66-77. PubMed ID: 2568752
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  • 10. Unique karyotypes in two patients with Prader-Willi syndrome.
    Narahara K, Hiramoto K, Murakami M, Miyake S, Tsuji K, Yokoyama Y, Namba H, Ninomiya S, Murakami R, Seino Y.
    Am J Med Genet; 1992 Mar 01; 42(5):671-7. PubMed ID: 1632436
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  • 13. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E, Biancalana V, Girard-Lemaire F, Favre R, Flori J, Doray B, Mandel JL.
    Eur J Hum Genet; 2004 Mar 01; 12(3):181-6. PubMed ID: 14694357
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  • 15. 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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  • 17. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):813-20. PubMed ID: 3688019
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  • 19. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD.
    Am J Med Genet; 1993 Oct 01; 47(5):683-6. PubMed ID: 8266996
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