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2. [Syndrome of congenital defects of the heart, eye and osseous system]. Szczeklik E, Strózyna-Kotulska W, Kustrzycki A, Olichwier B, Bross T. Przegl Lek; 1976; 33(4):479-81. PubMed ID: 818682 [No Abstract] [Full Text] [Related]
4. [Case of "upper limb-cardiovascular syndrome" (Holt-Oram syndrome)]. Polimeno M, Fadda C, Abate M, Morieri M, Del Vecchio E. Minerva Pediatr; 1982 Jun 15; 34(11):511-6. PubMed ID: 7132932 [No Abstract] [Full Text] [Related]
10. A case of Holt Oram syndrome. Abhayambika K, Girija G, Joseph J. Indian Heart J; 1991 Dec 15; 43(1):59-60. PubMed ID: 1894307 [No Abstract] [Full Text] [Related]
13. Reduction malformations and chromosome anomalies. Bofinger MK, Dignan PS, Schmidt RE, Warkany J. Am J Dis Child; 1973 Jan 15; 125(1):135-43. PubMed ID: 4346056 [No Abstract] [Full Text] [Related]
14. Syndrome of a craniofacial dysostosis, limb malformation, and omphalocele. Gardner RJ, Morrison PS, Faigan LA, Kennedy JC, Fitzgerald PH. Am J Med Genet; 1990 Jun 15; 36(2):133-6. PubMed ID: 2368799 [Abstract] [Full Text] [Related]
15. Congenital triangular alopecia in association with congenital heart diseases, bone and teeth abnormalities, multiple lentigines and café-au-lait patches. Park SW, Choi YD, Wang HY. Int J Dermatol; 2004 May 15; 43(5):366-7. PubMed ID: 15117369 [No Abstract] [Full Text] [Related]
16. Six generations of a family with multiple limb deficiencies. Helal A, Perry T, Ogden JA, Greene TL. J Pediatr Orthop; 1993 May 15; 13(2):210-3. PubMed ID: 8459013 [Abstract] [Full Text] [Related]