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Journal Abstract Search

238 related items for PubMed ID: 3688021

  • 1. 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]

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

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
    Gilhuis HJ, van Ravenswaaij CM, Hamel BJ, Gabreëls FJ.
    Eur J Paediatr Neurol; 2000 Sep 15; 4(1):39-43. PubMed ID: 10701104
    [Abstract] [Full Text] [Related]

  • 7. [Prader-Willi syndrome or Angelman syndrome? A question of maternal or paternal chromosome 15].
    Ritzén M, Anvret M.
    Lakartidningen; 1992 May 27; 89(22):1985-6. PubMed ID: 1630213
    [No Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.
    Williams CA, Gray BA, Hendrickson JE, Stone JW, Cantú ES.
    Am J Med Genet; 1989 Mar 01; 32(3):339-45. PubMed ID: 2786338
    [Abstract] [Full Text] [Related]

  • 10. [Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].
    Pfeiffer RA, Tschech L, Irle U, Wündisch GF.
    Klin Padiatr; 1987 Mar 01; 199(5):329-35. PubMed ID: 3316824
    [Abstract] [Full Text] [Related]

  • 11. Cytogenetic and molecular study of Angelman syndrome.
    Imaizumi K, Takada F, Kuroki Y, Naritomi K, Hamabe J, Niikawa N.
    Am J Med Genet; 1990 Mar 01; 35(3):314-8. PubMed ID: 2309778
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  • 13. 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 01; 32(2):285-90. PubMed ID: 2564739
    [Abstract] [Full Text] [Related]

  • 14. [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 01; 37(5):255-61. PubMed ID: 4023109
    [Abstract] [Full Text] [Related]

  • 15. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.
    Kaplan LC, Wharton R, Elias E, Mandell F, Donlon T, Latt SA.
    Am J Med Genet; 1987 Sep 01; 28(1):45-53. PubMed ID: 3674117
    [Abstract] [Full Text] [Related]

  • 16. 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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  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Angelman syndrome in a daughter with del(15) (q11q13) associated with brachycephaly, hearing loss, enlarged foramen magnum, and ataxia in the mother.
    Williams CA, Hendrickson JE, Cantú ES, Donlon TA.
    Am J Med Genet; 1989 Mar 11; 32(3):333-8. PubMed ID: 2729353
    [Abstract] [Full Text] [Related]

  • 20. Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.
    Williams CA, Zori RT, Stone JW, Gray BA, Cantu ES, Ostrer H.
    Am J Med Genet; 1990 Mar 11; 35(3):350-3. PubMed ID: 2309781
    [Abstract] [Full Text] [Related]

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