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Journal Abstract Search

149 related items for PubMed ID: 1630213

  • 1.
    ; . PubMed ID:
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  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
    Knoll JH, Nicholls RD, Magenis RE, Graham JM, Lalande M, Latt SA.
    Am J Med Genet; 1989 Feb; 32(2):285-90. PubMed ID: 2564739
    [Abstract] [Full Text] [Related]

  • 4.
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  • 5. Is Angelman syndrome an alternate result of del(15)(q11q13)?
    Magenis RE, Brown MG, Lacy DA, Budden S, LaFranchi S.
    Am J Med Genet; 1987 Dec; 28(4):829-38. PubMed ID: 3688021
    [Abstract] [Full Text] [Related]

  • 6. [Prader-Willi syndrome in 22-year-old man--case study].
    Kardas P, Adamiak-Kardas M.
    Wiad Lek; 2001 Dec; 54(11-12):709-14. PubMed ID: 11928560
    [Abstract] [Full Text] [Related]

  • 7. [Report of case of Prader-Willi syndrome].
    Visco G, Ughi M, Trevenzoli G.
    Pediatr Med Chir; 1999 Dec; 21(3):149-50. PubMed ID: 10687166
    [Abstract] [Full Text] [Related]

  • 8. Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromes.
    Zori R, Williams C, Mattei JF, Moncla A.
    Am J Med Genet; 1990 Oct; 37(2):294-5. PubMed ID: 2248305
    [No Abstract] [Full Text] [Related]

  • 9. Prader-Willi syndrome.
    Cassidy SB, Ledbetter DH.
    Neurol Clin; 1989 Feb; 7(1):37-54. PubMed ID: 2646521
    [Abstract] [Full Text] [Related]

  • 10. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G, Tükün A, Yalaz K, Bökesoy I.
    Turk J Pediatr; 1993 Feb; 35(4):333-6. PubMed ID: 8160287
    [Abstract] [Full Text] [Related]

  • 11. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome].
    Witkowski R, Ullrich E, Pietsch P, Weber K, Heller K, Losanowa T, Nitz I.
    Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109
    [Abstract] [Full Text] [Related]

  • 12. Family studies in Prader-Willi syndrome.
    Webb T, Hardy CA, Dahlitz M, Watkiss E, Clarke D.
    Genet Couns; 1994 May; 5(4):329-36. PubMed ID: 7888134
    [Abstract] [Full Text] [Related]

  • 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; 12(3):181-6. PubMed ID: 14694357
    [Abstract] [Full Text] [Related]

  • 14. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?
    Kim HJ, Cho HJ, Jin DK, Kwon EK, Ki CS, Kim JW, Kim SH.
    Clin Genet; 2004 Oct; 66(4):368-72. PubMed ID: 15355442
    [No Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.
    Toth-Fejel S, Magenis RE, Leff S, Brown MG, Comegys B, Lawce H, Berry T, Kesner D, Webb MJ, Olson S.
    Am J Med Genet; 1995 Feb 13; 55(4):444-52. PubMed ID: 7762584
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: an overview.
    Knoll JH, Wagstaff J, Lalande M.
    Am J Med Genet; 1993 Apr 01; 46(1):2-6. PubMed ID: 8388170
    [Abstract] [Full Text] [Related]

  • 18. Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes.
    Kirkilionis AJ, Chudley AE, Gregory CA, Hamerton JL.
    Am J Med Genet; 1991 Sep 15; 40(4):454-9. PubMed ID: 1684091
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  • 19.
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  • 20. Deletion and uniparental disomy involving the same maternal chromosome 15.
    Surh LC, Wang H, Hunter AG.
    N Engl J Med; 1994 Feb 24; 330(8):572-3. PubMed ID: 8302329
    [No Abstract] [Full Text] [Related]

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