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Journal Abstract Search
175 related items for PubMed ID: 7171780
21. Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosis. Opitz JM, Mollica F, Sorge G, Milana G, Cimino G, Caltabiano M. Am J Med Genet; 1993 Oct 01; 47(5):660-78. PubMed ID: 8266994 [Abstract] [Full Text] [Related]
23. TCOF1 mutations excluded from a role in other first and second branchial arch-related disorders. Splendore A, Passos-Bueno MR, Jabs EW, Van Maldergem L, Wulfsberg EA. Am J Med Genet; 2002 Aug 15; 111(3):324-7. PubMed ID: 12210332 [No Abstract] [Full Text] [Related]
24. [Anticipation and the Franceschetti-Zwahlen-Klein syndrome]. Le Marec B, Bourdiniere J, Jezequel J, Senecal J. J Genet Hum; 1974 Mar 15; 22(1):7-19. PubMed ID: 4430898 [No Abstract] [Full Text] [Related]
27. [3 cases of Goldenhar syndrome]. Lisicka E. Klin Oczna; 1984 Jun 15; 86(6):273-4. PubMed ID: 6438388 [No Abstract] [Full Text] [Related]
28. [Involvement of the inner ear in the Goldenhar syndrome. Study of 2 cases]. Calvani M, Marconi M, Bellussi A, Paolone G. Minerva Pediatr; 1979 Dec 15; 31(23):1699-710. PubMed ID: 554963 [No Abstract] [Full Text] [Related]