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

235 related items for PubMed ID: 31958577

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

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

  • 3. Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
    Huber J, Peres VC, de Castro AL, dos Santos TJ, da Fontoura Beltrão L, de Baumont AC, Cossio SL, Dalberto TP, Riegel M, Cañedo AD, Schaan BD, Pellanda LC.
    Pediatr Cardiol; 2014 Dec; 35(8):1356-62. PubMed ID: 24880467
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study.
    Ron HA, Crowley TB, Liu Y, Unolt M, Schindewolf E, Moldenhauer J, Rychik J, Goldmuntz E, Emanuel BS, Ryba D, Gaynor JW, Zackai EH, Hakonarson H, McDonald-McGinn DM.
    Genes (Basel); 2022 Dec 24; 14(1):. PubMed ID: 36672801
    [Abstract] [Full Text] [Related]

  • 8. Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome.
    Chan C, Costain G, Ogura L, Silversides CK, Chow EW, Bassett AS.
    J Genet Couns; 2015 Oct 24; 24(5):810-21. PubMed ID: 25579115
    [Abstract] [Full Text] [Related]

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

  • 10. 22q11.2 deletion syndrome and congenital heart disease.
    Goldmuntz E.
    Am J Med Genet C Semin Med Genet; 2020 Mar 24; 184(1):64-72. PubMed ID: 32049433
    [Abstract] [Full Text] [Related]

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

  • 12. Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.
    Liu AP, Chow PC, Lee PP, Mok GT, Tang WF, Lau ET, Lam ST, Chan KY, Kan AS, Chau AK, Cheung YF, Lau YL, Chung BH.
    Eur J Med Genet; 2014 Mar 24; 57(6):306-11. PubMed ID: 24721633
    [Abstract] [Full Text] [Related]

  • 13. Club foot in association with the 22q11.2 deletion syndrome: An observational study.
    Homans JF, Crowley TB, Chen E, McGinn DE, Deeney VFX, Sakkers RJB, Davidson RS, Castelein RM, McDonald-McGinn DM.
    Am J Med Genet A; 2018 Oct 24; 176(10):2135-2139. PubMed ID: 30380189
    [Abstract] [Full Text] [Related]

  • 14. Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.
    Butcher NJ, Kiehl TR, Hazrati LN, Chow EW, Rogaeva E, Lang AE, Bassett AS.
    JAMA Neurol; 2013 Nov 24; 70(11):1359-66. PubMed ID: 24018986
    [Abstract] [Full Text] [Related]

  • 15. Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients.
    León LE, Benavides F, Espinoza K, Vial C, Alvarez P, Palomares M, Lay-Son G, Miranda M, Repetto GM.
    Sci Rep; 2017 May 11; 7(1):1795. PubMed ID: 28496102
    [Abstract] [Full Text] [Related]

  • 16. Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
    Unolt M, Versacci P, Anaclerio S, Lambiase C, Calcagni G, Trezzi M, Carotti A, Crowley TB, Zackai EH, Goldmuntz E, Gaynor JW, Digilio MC, McDonald-McGinn DM, Marino B.
    Am J Med Genet A; 2018 Oct 11; 176(10):2087-2098. PubMed ID: 29663641
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Association of airway abnormalities with 22q11.2 deletion syndrome.
    Sacca R, Zur KB, Crowley TB, Zackai EH, Valverde KD, McDonald-McGinn DM.
    Int J Pediatr Otorhinolaryngol; 2017 May 11; 96():11-14. PubMed ID: 28390597
    [Abstract] [Full Text] [Related]

  • 19.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, McDonald-McGinn DM, Hain HS, Emanuel BS, Zackai EH.
    ; 1993 May 11. PubMed ID: 20301696
    [Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 12.