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.
42. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9. Butler LJ; Eades SM; France NE Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708 [No Abstract] [Full Text] [Related]
43. Malformative syndrome with ring chromosome 13. Fryns JP; Deoover J; Van den Berghe H Humangenetik; 1974; 24(3):235-40. PubMed ID: 4140834 [No Abstract] [Full Text] [Related]
44. An analysis of the parental age effect for inv dup (15). Connor JM; Gilmore DH J Med Genet; 1984 Jun; 21(3):213-4. PubMed ID: 6748017 [TBL] [Abstract][Full Text] [Related]
45. Interstitial deletion of the short arm of chromosome 4. Ray M; Evans J; Rockman-Greenberg C; Wickstrom D J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021 [TBL] [Abstract][Full Text] [Related]
46. Ring (15) chromosome. Yunis E; Leibovici M; Quintero L Hum Genet; 1981; 57(2):207-9. PubMed ID: 7228035 [TBL] [Abstract][Full Text] [Related]
47. SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214). Leschot NJ; Slater RM; Joenje H; Becker-Bloemkolk MJ; de Nef JJ Hum Genet; 1981; 57(2):220-3. PubMed ID: 7228038 [TBL] [Abstract][Full Text] [Related]
48. 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]
49. Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat. Moedjono SJ; Sparkes RS Hum Genet; 1979 Sep; 50(3):241-6. PubMed ID: 489007 [TBL] [Abstract][Full Text] [Related]
50. Subglottic pseudotumor, laryngeal dysplasia, and chondrodysplasia calcificans congenita with a t(D;B) chromosomal translocation. Valdmanis A; Wilson JR; Mann JD; Pearson G; Shaw MW Ann Genet; 1967 Jun; 10(2):55-9. PubMed ID: 5298973 [No Abstract] [Full Text] [Related]
51. A child trisomic for the distal part of chromosome 14q. Bridgman G; Butler LJ Arch Dis Child; 1980 Jun; 55(6):474-7. PubMed ID: 7436488 [TBL] [Abstract][Full Text] [Related]
52. De novo 13q paracentric inversion in a boy with cleft palate and mental retardation. Riccardi VM; Holmquist GP Hum Genet; 1979 Nov; 52(2):211-5. PubMed ID: 511176 [TBL] [Abstract][Full Text] [Related]
53. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci. Bernstein R; Dawson B; Kohl R; Jenkins T J Med Genet; 1979 Aug; 16(4):254-62. PubMed ID: 290816 [TBL] [Abstract][Full Text] [Related]
54. Neurological and neuropathological findings in ring chromosome 4. Young RS; Zalneraitis EL J Med Genet; 1980 Dec; 17(6):487-90. PubMed ID: 7205435 [TBL] [Abstract][Full Text] [Related]
55. Human chromosome abnormalities as related to physical and mental dysfunction. Heller JH J Hered; 1969; 60(5):239-48. PubMed ID: 4244249 [No Abstract] [Full Text] [Related]
56. The results of chromosome examinations in an institution for mental retardates in the Cape Province. Nelson MM; Smart RD S Afr Med J; 1982 Jul; 62(1):25-9. PubMed ID: 7089776 [TBL] [Abstract][Full Text] [Related]
57. Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion. Funderburk SJ; Crandall BF Am J Hum Genet; 1974 Nov; 26(6):715-22. PubMed ID: 4140688 [No Abstract] [Full Text] [Related]
58. 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]
59. Karyotype with chromosomal abnormality with various inherited defects in the offspring (recombination aneusomy). Warter S; Ruch JV; Lehmann M Humangenetik; 1973 Dec; 20(4):355-9. PubMed ID: 4768111 [No Abstract] [Full Text] [Related]