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22. A hereditary bisatellite-dicentric supernumerary chromosome in a case of cat-eye syndrome. Lüleci G; Bağci G; Kivran M; Lüleci E; Bektaş S; Başaran S Hereditas; 1989; 111(1):7-10. PubMed ID: 2793513 [TBL] [Abstract][Full Text] [Related]
24. Updating advances in cytogenetics. Applications of the new chromosome banding methods. Breg WR Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402 [No Abstract] [Full Text] [Related]
25. Chromosome survey of moderately to profoundly retarded patients. Carrel RE; Sparkes RS; Wright SW Am J Ment Defic; 1973 Mar; 77(5):616-22. PubMed ID: 4703994 [No Abstract] [Full Text] [Related]
26. [X-chromosome translocations. Examination based on treatment with BUDR and staining with acridine orange]. Dutrillaux B; Laurent C; Gilgenkrantz S; Frédéric J; Carpentier S; Couturier J; Lejeune J Helv Paediatr Acta; 1974; Suppl 34():19-31. PubMed ID: 4141698 [No Abstract] [Full Text] [Related]
27. The "cat eye" syndrome--report of a case with hypothyroidism. Ioan D; Dumitriu L; Fabriţius K; Simescu M; Maximilian C Endocrinologie; 1986; 24(2):129-31. PubMed ID: 3738402 [TBL] [Abstract][Full Text] [Related]
30. Midtrimester diagnosis and anomalies in the dup(22q) syndrome: correlation of aneuploidy with low maternal serum alpha-fetoprotein and oligohydramnios. Johnson MP; Greb A; Goyert G; Drugan A; Qureshi F; Sacks AJ; Evans MI Am J Med Genet; 1990 May; 36(1):94-6. PubMed ID: 1692182 [TBL] [Abstract][Full Text] [Related]
31. [Children with chromosome abnormalities in a pediatric department]. Nielsen J; Friedrich U; Holm V; Sveinsson S Ugeskr Laeger; 1973 Feb; 135(8):408-15. PubMed ID: 4265917 [No Abstract] [Full Text] [Related]
35. [Mental retardation: genetic counseling and prenatal diagnosis]. Engel E Rev Med Suisse Romande; 1981 May; 101(5):341-6. PubMed ID: 7291823 [No Abstract] [Full Text] [Related]
36. [Crying cat syndrome. Lejeune's syndrome. 5p-. Monosomi short arm 5]. Niebuhr E Ugeskr Laeger; 1971 Jun; 133(23):1130. PubMed ID: 5556617 [No Abstract] [Full Text] [Related]
37. Cat eye syndrome associated with aganglionosis of the small and large intestine. Ward J; Sierra IA; D'Croz E J Med Genet; 1989 Oct; 26(10):647-8. PubMed ID: 2585462 [TBL] [Abstract][Full Text] [Related]
38. Genetic screening for mental retardation in Michigan. Thoene J; Higgins J; Krieger I; Schmickel R; Weiss L Am J Ment Defic; 1981 Jan; 85(4):335-40. PubMed ID: 7457497 [TBL] [Abstract][Full Text] [Related]
39. [Peculiar findings in G group chromosome aberrations]. Grünwald P; Schweikhardt F Acta Genet Med Gemellol (Roma); 1969 Jan; 18(1):92-8. PubMed ID: 4240534 [No Abstract] [Full Text] [Related]
40. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders]. Kuleshov NP; Zaletaev DV; Levina LIa; Dement'eva GM; Arbuzov SP Tsitol Genet; 1985; 19(6):452-6. PubMed ID: 4089954 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]