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7. Interstitial deletion of 11q. Guć-Sćekić M, Pilić-Radivojević G, Mrdjenović G, Djurić M. J Med Genet; 1989 Mar; 26(3):205-6. PubMed ID: 2468775 [No Abstract] [Full Text] [Related]
8. Del(4)(q33----qter): another case report of a child with mild dysmorphism. Fagan KA, Morris RB. J Med Genet; 1989 Dec; 26(12):776-8. PubMed ID: 2614797 [Abstract] [Full Text] [Related]
14. An apparent de novo terminal deletion of chromosome 2 (pter----p24:). Francis GL, Flannery DB, Byrd JR, Fisher ST. J Med Genet; 1990 Feb; 27(2):137-8. PubMed ID: 2319584 [No Abstract] [Full Text] [Related]
15. Difficulties encountered in the clinical description of the dysmorphic patient. Feingold M. J Craniofac Genet Dev Biol; 1989 Feb; 9(1):3-5. PubMed ID: 2794001 [No Abstract] [Full Text] [Related]
16. [Ring chromosome 14. I. A case report on homogeneous r(14)]. Raoul O, Razavi F, Lescs MC, Bouhanna A. Ann Genet; 1984 Feb; 27(2):88-90. PubMed ID: 6331795 [Abstract] [Full Text] [Related]