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26. Unilateral absent scaphoid in a patient with "Holt-Oram" syndrome. De Smet L Genet Couns; 2002; 13(3):327-9. PubMed ID: 12416641 [TBL] [Abstract][Full Text] [Related]
27. [Holt-Oram syndrome with malformations of the urinary system]. Dogliani P; De Sanctis C; Balocco A Minerva Pediatr; 1973 Jun; 25(23):1002-6. PubMed ID: 4745024 [No Abstract] [Full Text] [Related]
28. A girl with severe expression of the holt-oram gene. Gardner RJ; Buckfield PM; Veale AM Clin Genet; 1973; 4(5):417-21. PubMed ID: 4751311 [No Abstract] [Full Text] [Related]
29. A case of Holt-Oram syndrome severely affecting the skeleton of the upper limbs. Cevik N; Cevik N; Bilgiç A Turk J Pediatr; 1985; 27(1):25-32. PubMed ID: 3984053 [No Abstract] [Full Text] [Related]
30. [The Holt-Oram syndrome. Description of a family group]. Politi G; Braguzzi E; Aitini E; Copelli T; Cacioli D; Diocleziani P; Grio V Minerva Cardioangiol; 1981 Oct; 29(10):575-90. PubMed ID: 6459539 [No Abstract] [Full Text] [Related]
31. [Case of "upper limb-cardiovascular syndrome" (Holt-Oram syndrome)]. Polimeno M; Fadda C; Abate M; Morieri M; Del Vecchio E Minerva Pediatr; 1982 Jun; 34(11):511-6. PubMed ID: 7132932 [No Abstract] [Full Text] [Related]
33. [Pulmonary hypertension in septal defects and its significance in determining indications for surgery]. Solov'ev GM; Korotkov AA; Mogilevskiĭ EB Grudn Khir; 1970; 12(2):36-41. PubMed ID: 5451650 [No Abstract] [Full Text] [Related]
34. Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q. Terrett JA; Newbury-Ecob R; Cross GS; Fenton I; Raeburn JA; Young ID; Brook JD Nat Genet; 1994 Apr; 6(4):401-4. PubMed ID: 8054982 [TBL] [Abstract][Full Text] [Related]
35. [Intracardiac phonocardiography as an aid to diagnosis of heart septal defects]. Rautenburg HW; Menner K Cardiologia (Basel); 1967; 51(6):359-68. PubMed ID: 5613030 [No Abstract] [Full Text] [Related]
36. [Pacemaker in Holt-Oram syndrome]. Seling A Zentralbl Chir; 1968 Oct; 93(42):1488-92. PubMed ID: 5725666 [No Abstract] [Full Text] [Related]
37. [The Holt-Oram syndrome. Entelechy or clinical entity? A mild form of familial presentation]. Palma Nieto JC; Herráez García J; Sciaccaluga Morelli C; Briones García JL Rev Esp Cardiol; 1993 Jun; 46(6):385-8. PubMed ID: 8316706 [TBL] [Abstract][Full Text] [Related]
38. [Holt-Oram syndrome. Description of a case]. Solarino M; Brindicci G; Donadeo V; Laforgia R Radiol Med; 1993 Oct; 86(4):548-50. PubMed ID: 8248601 [No Abstract] [Full Text] [Related]
39. [An unusual type of congenital heart disease associated with the Holt-Oram-syndrome (author's transl)]. Ruzić B; Bosnar B; Beleznay O Radiologe; 1981 Jun; 21(6):296-9. PubMed ID: 7268028 [TBL] [Abstract][Full Text] [Related]