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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

301 related items for PubMed ID: 28807863

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  • 24. Radial Ray Malformation.
    Society for Maternal-Fetal Medicine (SMFM), Gandhi M, Rac MWF, McKinney J.
    Am J Obstet Gynecol; 2019 Dec; 221(6):B16-B18. PubMed ID: 31787159
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  • 25. [Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier].
    Murga-Eizagaechevarria N, Garcia-Barcina M, Sarasola Diez E.
    Rev Esp Cardiol; 2011 Dec; 64(12):1225-6. PubMed ID: 21752519
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  • 27. A novel missense mutation in the TBX5 gene in a Saudi infant with Holt-Oram syndrome.
    Al-Qattan MM, Abou Al-Shaar H.
    Saudi Med J; 2015 Aug; 36(8):980-2. PubMed ID: 26219450
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  • 29. Xq26.3 microdeletion in a male with Wildervanck Syndrome.
    Abu-Amero KK, Kondkar AA, Alorainy IA, Khan AO, Al-Enazy LA, Oystreck DT, Bosley TM.
    Ophthalmic Genet; 2014 Mar; 35(1):18-24. PubMed ID: 23373430
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  • 30. Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants.
    Vanlerberghe C, Jourdain AS, Ghoumid J, Frenois F, Mezel A, Vaksmann G, Lenne B, Delobel B, Porchet N, Cormier-Daire V, Smol T, Escande F, Manouvrier-Hanu S, Petit F.
    Eur J Hum Genet; 2019 Mar; 27(3):360-368. PubMed ID: 30552424
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  • 35. Molecular basis of the clinical features of Holt-Oram syndrome resulting from missense and extended protein mutations of the TBX5 gene as well as TBX5 intragenic duplications.
    Al-Qattan MM, Abou Al-Shaar H.
    Gene; 2015 Apr 15; 560(2):129-36. PubMed ID: 25680289
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  • 38. Possible Holt-Oram Syndrome: Missed Prenatal Diagnosis and Sub-Optimal Management in a Poor-Resourced Hospital.
    Osonuga A, Arhin JK, Okoye GC, Da’Costa A.
    Balkan Med J; 2019 May 10; 36(3):192-193. PubMed ID: 30873826
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  • 39. Functional analysis of two novel TBX5 variants present in individuals with Holt-Oram syndrome with different clinical manifestations.
    Varela D, Varela T, Conceição N, Ferreira Â, Marques N, Silva AP, Azevedo P, Pereira S, Camacho A, de Jesus I, Cancela ML.
    Mol Genet Genomics; 2021 Jul 10; 296(4):809-821. PubMed ID: 33866394
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