These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

296 related items for PubMed ID: 18307085

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Congenital heart disease: Molecular diagnostics of supravalvular aortic stenosis.
    Tassabehji M, Urban Z.
    Methods Mol Med; 2006; 126():129-56. PubMed ID: 16930010
    [Abstract] [Full Text] [Related]

  • 5. Elastin: mutational spectrum in supravalvular aortic stenosis.
    Metcalfe K, Rucka AK, Smoot L, Hofstadler G, Tuzler G, McKeown P, Siu V, Rauch A, Dean J, Dennis N, Ellis I, Reardon W, Cytrynbaum C, Osborne L, Yates JR, Read AP, Donnai D, Tassabehji M.
    Eur J Hum Genet; 2000 Dec; 8(12):955-63. PubMed ID: 11175284
    [Abstract] [Full Text] [Related]

  • 6. Biomechanical Description of Phonation in Children Affected by Williams Syndrome.
    Hidalgo I, Gómez Vilda P, Garayzábal E.
    J Voice; 2018 Jul; 32(4):515.e15-515.e28. PubMed ID: 28779989
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Supravalvular aortic stenosis: genetic and molecular dissection of a complex mutation in the elastin gene.
    Urbán Z, Zhang J, Davis EC, Maeda GK, Kumar A, Stalker H, Belmont JW, Boyd CD, Wallace MR.
    Hum Genet; 2001 Nov; 109(5):512-20. PubMed ID: 11735026
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Williams syndrome and the elastin gene in Thai patients.
    Ruangdaraganon N, Tocharoentanaphol C, Kotchabhakdi N, Khowsathit P.
    J Med Assoc Thai; 1999 Nov; 82 Suppl 1():S174-8. PubMed ID: 10730539
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Spectral analysis of the voice in Down Syndrome.
    Albertini G, Bonassi S, Dall'Armi V, Giachetti I, Giaquinto S, Mignano M.
    Res Dev Disabil; 2010 Nov; 31(5):995-1001. PubMed ID: 20488659
    [Abstract] [Full Text] [Related]

  • 15. Genetic Diagnosis and the Severity of Cardiovascular Phenotype in Patients With Elastin Arteriopathy.
    Min S, Kinnear C, D'Alessandro LCA, Bouwmeester J, Yao R, Chiasson D, Keeley F, Mital S.
    Circ Genom Precis Med; 2020 Dec; 13(6):e002971. PubMed ID: 32960096
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Vocal cord abnormalities in Williams syndrome: a further manifestation of elastin deficiency.
    Vaux KK, Wojtczak H, Benirschke K, Jones KL.
    Am J Med Genet A; 2003 Jun 15; 119A(3):302-4. PubMed ID: 12784297
    [Abstract] [Full Text] [Related]

  • 18. Acoustic measures and self-reports of vocal fatigue by female teachers.
    Laukkanen AM, Ilomäki I, Leppänen K, Vilkman E.
    J Voice; 2008 May 15; 22(3):283-9. PubMed ID: 17134877
    [Abstract] [Full Text] [Related]

  • 19. [Cardiovascular manifestations in 40 patients with Williams syndrome].
    Xie CH, Zhao ZY, Yang JB, Qin YF, Shao J, Gong FQ.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2007 Oct 15; 35(10):904-7. PubMed ID: 18206036
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.