These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
158 related articles for article (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]
6. [Cat eye syndrome with pituitary dwarfism and normal mental development]. Pierson M; Gilgenkrantz S; Saborio M Arch Fr Pediatr; 1975 Nov; 32(9):835-48. PubMed ID: 1217955 [TBL] [Abstract][Full Text] [Related]
7. Dermatoglyphics and chromosomes in cat-eye syndrome. Dallapiccola B Br Med J; 1971 Sep; 3(5777):767-8. PubMed ID: 5097980 [No Abstract] [Full Text] [Related]
8. Inverted duplication of 22pter----q11.21 in cat-eye syndrome. Hoo JJ; Robertson A; Fowlow SB; Bowen P; Lin CC Am J Med Genet; 1986 Jul; 24(3):543-5. PubMed ID: 3728573 [No Abstract] [Full Text] [Related]
9. [Coloboma and anal atresia: phenotype of a chromosome aberration?]. Pfeiffer RA; Heimann K; Heiming E; Schlack H; Maul H Klin Monbl Augenheilkd; 1971 Sep; 159(3):357-67. PubMed ID: 5003627 [No Abstract] [Full Text] [Related]
10. Extra chromosome in "cat eye" syndrome. Pfeiffer RA; Heimann K; Heiming E Lancet; 1970 Jul; 1(7663):97. PubMed ID: 4193380 [No Abstract] [Full Text] [Related]
11. Case report. The cat-eye syndrome with unusual skeletal malformations. Balci S; Halicioglu C; Say B; Taysi K Acta Paediatr Scand; 1974 Jul; 63(4):623-6. PubMed ID: 4850902 [No Abstract] [Full Text] [Related]
12. [Complex cyanotic heart defect in a newborn infant with cat eye syndrome]. Paul T; Reimer A; Wilken M; Miller K; Kallfelz HC Monatsschr Kinderheilkd; 1991 Apr; 139(4):228-30. PubMed ID: 2072964 [TBL] [Abstract][Full Text] [Related]
14. Structural variation in human nitotic chromosomes. Leisti J Ann Acad Sci Fenn Biol; 1971; 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; 131(8):893-97. PubMed ID: 888806 [TBL] [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; 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; 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; 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; 3(2):135-46. PubMed ID: 5054315 [No Abstract] [Full Text] [Related]
20. [Extra mini-chromosome with symptoms of cat-eye syndrome]. Méhes K; Bajnóczky K; Schmidt P Orv Hetil; 1985 Apr; 126(17):1037-9. PubMed ID: 3991187 [No Abstract] [Full Text] [Related] [Next] [New Search]