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42. An inherited 1;G translocation. Ebbin AJ; Wilson MG; Towner JW; Forsman I J Med Genet; 1971 Dec; 8(4):536-9. PubMed ID: 5149540 [No Abstract] [Full Text] [Related]
43. Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies. Kakati S; Sinha AK Hum Hered; 1973 Apr; 23(4):313-30. PubMed ID: 4130026 [No Abstract] [Full Text] [Related]
44. Ring chromosome 14: a distinct clinical entity. Schmidt R; Eviatar L; Nitowsky HM; Wong M; Miranda S J Med Genet; 1981 Aug; 18(4):304-7. PubMed ID: 7277427 [TBL] [Abstract][Full Text] [Related]
45. A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations. van Hemel JO; van Biervliet JP; de Jager-van der Grift PW Clin Genet; 1975 Sep; 8(3):213-7. PubMed ID: 1175325 [No Abstract] [Full Text] [Related]
46. Ring chromosome 18 in a patient with multiple anomalies. Palmer CG; Fareed N; Merritt AD J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991 [No Abstract] [Full Text] [Related]
47. Pericentric inversion of chromosome 11 in one of two similar retarded brothers. Einfeld SL; Smith A J Med Genet; 1982 Aug; 19(4):312. PubMed ID: 7120323 [No Abstract] [Full Text] [Related]
48. [The chromosomal syndromes (author's transl)]. Klein D Padiatr Padol Suppl; 1975; 4():1-31. PubMed ID: 127145 [TBL] [Abstract][Full Text] [Related]
50. A profoundly mentally handicapped woman with a ring chromosome 22. Veall RM; Rundle AT; Chitham RC; Saldana-Garcia P J Ment Defic Res; 1975; 19(3-4):225-43. PubMed ID: 1214291 [TBL] [Abstract][Full Text] [Related]
51. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome. Visfeldt J Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134 [No Abstract] [Full Text] [Related]
52. Sex chromatin survey among mentally retarded children in Japan. Yanagisawa S; Shuto T J Ment Defic Res; 1970 Sep; 14(3):254-62. PubMed ID: 5518410 [No Abstract] [Full Text] [Related]
53. Gene deletion and duplication effects on phenotype and gamma globulin levels. Rudd NL; Lamarche PH J Med Genet; 1971 Mar; 8(1):97-106. PubMed ID: 5098075 [No Abstract] [Full Text] [Related]
54. Familial cases of marker chromosomes of groups 21-22 and 13-15 (Gpss and Dp+). Kyaosaar ME Sov Genet; 1973 Nov; 7(7):913-8. PubMed ID: 4777944 [No Abstract] [Full Text] [Related]