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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

235 related items for PubMed ID: 19890921

  • 21.
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  • 22. Clinical features of 149 patients with facio-auriculo-vertebral spectrum.
    Muñoz-Pedroza LA, Arenas-Sordo ML.
    Acta Otorrinolaringol Esp; 2013; 64(5):359-62. PubMed ID: 23896491
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  • 23. OTX2 duplications: a recurrent cause of oculo-auriculo-vertebral spectrum.
    Celse T, Tingaud-Sequeira A, Dieterich K, Siegfried G, Lecaignec C, Bouneau L, Fannemel M, Salaun G, Laffargue F, Martinez G, Satre V, Vieville G, Bidart M, Soussi Zander C, Turesson AC, Splitt M, Reboul D, Chiesa J, Khau Van Kien P, Godin M, Gruchy N, Goel H, Palmer E, Demetriou K, Shalhoub C, Rooryck C, Coutton C.
    J Med Genet; 2023 Jun; 60(6):620-626. PubMed ID: 36368868
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  • 24. Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997-2019.
    Thomas MA, Bedard T, Crawford S, Lowry RB.
    Am J Med Genet A; 2024 Aug; 194(8):e63594. PubMed ID: 38553895
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  • 26. Hemifacial microsomia: skeletal abnormalities evaluation using CBCT (case report).
    Kabak SL, Savrasova NA, Zatochnaya VV, Melnichenko YM.
    J Radiol Case Rep; 2019 Nov; 13(11):1-9. PubMed ID: 32190180
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  • 36. Cranial Nerve Abnormalities in Oculo-Auriculo-Vertebral Spectrum.
    Manara R, Brotto D, Ghiselli S, Mardari R, Toldo I, Schifano G, Cantone E, Bovo R, Martini A.
    AJNR Am J Neuroradiol; 2015 Jul; 36(7):1375-80. PubMed ID: 25814660
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  • 37. Characterization of facial paresis in hemifacial microsomia.
    Cline JM, Hicks KE, Patel KG.
    Otolaryngol Head Neck Surg; 2014 Feb; 150(2):188-93. PubMed ID: 24492209
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  • 39. Persistent fifth aortic arch associated with 22q11.2 deletion syndrome.
    Lee ML, Chen HN, Chen M, Tsao LY, Wang BT, Lee MH, Chiu IS.
    J Formos Med Assoc; 2006 Apr; 105(4):284-9. PubMed ID: 16618608
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