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Journal Abstract Search
195 related items for PubMed ID: 4232527
21. Familial extra centric bisatellited chromosome. Armendares S, Buentello L, Cuevas-Sosa A, Cantú-Garza JM. Cytogenetics; 1969; 8(3):177-86. PubMed ID: 4240817 [No Abstract] [Full Text] [Related]
22. Down's syndrome. I. Cytogenetics. Maximilian C, Duca D, Pop T, Toncescu N, Ioan D. Endocrinologie; 1980; 18(4):273-5. PubMed ID: 6451918 [Abstract] [Full Text] [Related]
23. [The significance of association of satellited chromosomes]. Rosenkranz W, Fleck S. Humangenetik; 1969; 7(1):9-21. PubMed ID: 4238958 [No Abstract] [Full Text] [Related]
24. Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis. Caspersson T, Hultén M, Lindsten J, Therkelsen AJ, Zech L. Hereditas; 1971; 67(2):213-20. PubMed ID: 4142007 [No Abstract] [Full Text] [Related]
25. A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy. Orye E, Verhaaren H. Ann Genet; 1974 Sep; 17(3):217-20. PubMed ID: 4141590 [No Abstract] [Full Text] [Related]
26. Satellite associations of D group chromosomes in translocation carriers. Nakagome Y, Bloom AD. J Med Genet; 1970 Dec; 7(4):371-3. PubMed ID: 5501702 [No Abstract] [Full Text] [Related]
27. X chromosome long arm deletion in a patient with Down's syndrome. Luthardt FW, Palmer CG. J Med Genet; 1971 Sep; 8(3):387-91. PubMed ID: 4255466 [No Abstract] [Full Text] [Related]
31. Autoradiographic study of DNA synthesis in homologous chromosomes distinguishable by morphology. De Capoa A, Rocchi A, Miller DA, Miller OJ. Cytogenetics; 1971 Sep; 10(6):427-35. PubMed ID: 5146419 [No Abstract] [Full Text] [Related]
36. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+). Wyandt HE, Hecht F, Lovrien EW, Stewart RE. Cytogenetics; 1971 Sep; 10(6):413-26. PubMed ID: 5146418 [No Abstract] [Full Text] [Related]
37. Compensatory mechanisms in the satellite association patterns of individuals with Robertsonian translocations. Hansson A. Hereditas; 1975 Sep; 81(1):101-12. PubMed ID: 127767 [No Abstract] [Full Text] [Related]