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2. [Holt-Oram syndrome. Review and report of 2 clinical cases in a family]. Lima M Rev Port Cardiol; 1995 Mar; 14(3):265-6. PubMed ID: 7646665 [No Abstract] [Full Text] [Related]
3. [Characteristics of Holt-Oram syndrome]. Rozenberg VD Ter Arkh; 1987; 59(4):135-6. PubMed ID: 3589990 [No Abstract] [Full Text] [Related]
4. [Familial form of Holt-Oram syndrome]. Grabowska-Lubaszko U; Swiatkowska A; Balcerska A Pediatr Pol; 1978 Jan; 53(1):105-7. PubMed ID: 643396 [No Abstract] [Full Text] [Related]
5. [Deformities of the extremities in Holt-Oram syndrome]. Hupfauer W; Seling A Z Orthop Ihre Grenzgeb; 1971 May; 109(2):270-6. PubMed ID: 4254058 [No Abstract] [Full Text] [Related]
6. [Holt-Oram syndrome (apropos of a familial case concerning 5 generations)]. Giraud F; Bertozzi JB; Mattei JF; Gerard R; Bernard R Arch Fr Pediatr; 1974 Oct; 31(8):765-74. PubMed ID: 4462497 [No Abstract] [Full Text] [Related]
7. [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]
8. [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]
17. 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]
18. [Cardiomelic syndrome (Holt-Oram syndrome) in a 5-year old girl]. Augustínová A Cesk Pediatr; 1974 Dec; 29(12):643-5. PubMed ID: 4461175 [No Abstract] [Full Text] [Related]
19. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome). Basson CT; Cowley GS; Solomon SD; Weissman B; Poznanski AK; Traill TA; Seidman JG; Seidman CE N Engl J Med; 1994 Mar; 330(13):885-91. PubMed ID: 8114858 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]