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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 3812530)

  • 21. 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; 560(2):129-36. PubMed ID: 25680289
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Holt-Oram syndrome: an observation in a father and a son.
    Mekanandha V; Subhannachart W; Hathirat S
    J Med Assoc Thai; 1979 May; 62(5):272-6. PubMed ID: 438692
    [No Abstract]   [Full Text] [Related]  

  • 23. A new mutation in the TBX5 gene in Holt-Oram syndrome: two cases in the same family and prenatal diagnosis.
    Atik T; Dervisoglu H; Onay H; Ozkinay F; Cogulu O
    J Trop Pediatr; 2014 Jun; 60(3):257-9. PubMed ID: 24408148
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prolapsed mitral valve associated with the Holt-Oram syndrome.
    Miller AB; Salcedo EE; Bahler RC
    Chest; 1975 Feb; 67(2):230-2. PubMed ID: 1116403
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Characteristics of Holt-Oram syndrome].
    Rozenberg VD
    Ter Arkh; 1987; 59(4):135-6. PubMed ID: 3589990
    [No Abstract]   [Full Text] [Related]  

  • 26. [Holt-Oram syndrome].
    Kullmann F; Grimm T
    Dtsch Med Wochenschr; 1993 Oct; 118(40):1455-62. PubMed ID: 8404501
    [No Abstract]   [Full Text] [Related]  

  • 27. Holt-Oram syndrome in a Maltese family.
    Fenech FF; Jaccarini CJ; Agius PV
    Postgrad Med J; 1971 Sep; 47(551):589-94. PubMed ID: 5098916
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Holt-Oram syndrome.
    Smith AT; Sack GH; Taylor GJ
    J Pediatr; 1979 Oct; 95(4):538-43. PubMed ID: 480027
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Report of a family with Holt-Oram syndrome (author's transl)].
    Gaul G; Titscher G; Brand O; Heeger H
    Z Kardiol; 1979 Mar; 68(3):173-5. PubMed ID: 442759
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pathogenetic implications of muscular ventricular septal defect in Holt-Oram syndrome.
    Kumar A; Van Mierop LH; Epstein ML
    Am J Cardiol; 1994 May; 73(13):993-5. PubMed ID: 8184867
    [No Abstract]   [Full Text] [Related]  

  • 31. Absent Left Main Coronary Artery and Separate Ostia of Left Coronary System in a Patient with Holt-Oram Syndrome and Sinus Node Dysfunction.
    Aung TT; Roberto ES; Wase A
    Am J Case Rep; 2016 Feb; 17():93-6. PubMed ID: 26882979
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Holt-Oram syndrome and hand malformations associated with congenital heart disease].
    Pernot C; Dupuis C; Gilgenkrantz S; Hueber JM
    Arch Mal Coeur Vaiss; 1970 Oct; 63(10):1428-44. PubMed ID: 4993644
    [No Abstract]   [Full Text] [Related]  

  • 33. Associated skeletal and cardiac abnormalities: the Holt-Oram syndrome.
    Ashby DW; Chadha JS; Henderson CB
    Q J Med; 1969 Jul; 38(151):267-76. PubMed ID: 5343603
    [No Abstract]   [Full Text] [Related]  

  • 34. An operated case of Holt-Oram syndrome with autosomal dominant inheritance.
    Czakó Z; Gömöry A; Homolay P; Bacsa S; Kiss S; Móricz F; Fülöp F; Papp Z
    Basic Res Cardiol; 1976; 71(1):60-7. PubMed ID: 1259686
    [TBL] [Abstract][Full Text] [Related]  

  • 35. TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
    Guo DF; Li RG; Yuan F; Shi HY; Hou XM; Qu XK; Xu YJ; Zhang M; Liu X; Jiang JQ; Yang YQ; Qiu XB
    Mol Med Rep; 2016 May; 13(5):4349-56. PubMed ID: 27035640
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Variation in severity of cardiac disease in Holt-Oram syndrome.
    Sletten LJ; Pierpont ME
    Am J Med Genet; 1996 Oct; 65(2):128-32. PubMed ID: 8911604
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Left Ventricular Non-compaction in Holt-Oram Syndrome.
    Kapadia R; Choudhary P; Collins N; Celermajer D; Puranik R
    Heart Lung Circ; 2016 Jun; 25(6):626-30. PubMed ID: 26874791
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rare cardiac defect in Holt-Oram syndrome.
    Sinha R; Nema C
    Cardiovasc J Afr; 2012 Mar; 23(2):e3-4. PubMed ID: 22447508
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Variability of the Holt-Oram syndrome in Saudi individuals.
    Najjar H; Mardini M; Tabbaa R; Nyhan WL
    Am J Med Genet; 1988 Apr; 29(4):851-5. PubMed ID: 3400729
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Holt-Oram syndrome. Presentation of two cases (author's transl)].
    Ferriols Gil EJ; Fayos Soler JL; Elorza Arizmendi J; Alvarez Angel V
    An Esp Pediatr; 1981 Oct; 15(4):378-82. PubMed ID: 7337303
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.