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Journal Abstract Search
159 related items for PubMed ID: 5082091
1. A newborn with the cat-eye syndrome. Fryns JP, Eggermont E, Veresen H, Van den Berghe H. Humangenetik; 1972; 15(3):242-8. PubMed ID: 5082091 [No Abstract] [Full Text] [Related]
14. Structural variation in human nitotic chromosomes. Leisti J. Ann Acad Sci Fenn Biol; 1971 Sep 03; 179():1-69. PubMed ID: 4261167 [No Abstract] [Full Text] [Related]
15. Cat eye syndrome. Partial trisomy 22 due to translocation in the mother. Bofinger MK, Soukup SW. Am J Dis Child; 1977 Aug 03; 131(8):893-97. PubMed ID: 888806 [Abstract] [Full Text] [Related]
16. The cat-eye syndrome. Review and two further cases occurring in female siblings with normal chromosomes. Franklin RC, Parslow MI. Acta Paediatr Scand; 1972 Sep 03; 61(5):581-6. PubMed ID: 4626468 [No Abstract] [Full Text] [Related]
17. Duplication deficiency syndrome in familial translocation (2q-;5p+). Bijlsma JB, de France H, Bleeker-Wagemakers EM. Humangenetik; 1971 Sep 03; 12(2):110-22. PubMed ID: 5568729 [No Abstract] [Full Text] [Related]
18. ["Cat eye syndrome" with right renal agenesis. Report of a case and review of the literature]. Legros y Carrenard JR, Martínez Cortés F, Martín Sánchez J. An Esp Pediatr; 1992 Apr 03; 36(4):317-9. PubMed ID: 1605422 [No Abstract] [Full Text] [Related]
19. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome. Gustavson KH, Hitrec V, Santesson B. Clin Genet; 1972 Apr 03; 3(2):135-46. PubMed ID: 5054315 [No Abstract] [Full Text] [Related]