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2. The chromosome, its anatomy, and its aberrations. Yang-Feng TL Res Publ Assoc Res Nerv Ment Dis; 1991; 69():19-38. PubMed ID: 2003160 [No Abstract] [Full Text] [Related]
3. Human chromosome analysis: methodology and applications. Larson L Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140 [TBL] [Abstract][Full Text] [Related]
4. Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old children. Lubs HA; Patil SR; Kimberling WJ; Brown J; Cohen MM; Gerald PS; Hecht F; Moorhead P; Myrianthopoulos NC; Summit RL Birth Defects Orig Artic Ser; 1979; 15(1):191-202. PubMed ID: 444641 [No Abstract] [Full Text] [Related]
5. Cytogenetic studies by chromosome banding techniques on peripheral blood cells from nasopharyngeal carcinoma patients. Zhang SZ; Qiu JC; Gao XK; Lin DC; Liu YH; Xu LR Chin Med J (Engl); 1980 Apr; 93(4):251-9. PubMed ID: 6768525 [No Abstract] [Full Text] [Related]
6. An International System for Human Cytogenetic Nomenclature (1985) ISCN 1985. Report of the Standing Committee on Human Cytogenetic Nomenclature. Birth Defects Orig Artic Ser; 1985; 21(1):1-117. PubMed ID: 4041569 [No Abstract] [Full Text] [Related]
7. The loss of centromeric heterochromatin from an inactivated centromere of a dicentric chromosome. Nakagome Y; Nakahori Y; Mitani K; Matsumoto M Jinrui Idengaku Zasshi; 1986 Mar; 31(1):21-6. PubMed ID: 3735755 [No Abstract] [Full Text] [Related]
8. [Development of cytogenetic methodology: contributions to the knowledge of chromosome structure and its application in clinical practice]. Salamanca-Gómez F Gac Med Mex; 1983 Aug; 119(8):315-25. PubMed ID: 6680106 [No Abstract] [Full Text] [Related]
9. [Ring chromosome 13 and multiple malformations (author's transl)]. Antich J; Plaza J; Geán E An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149 [TBL] [Abstract][Full Text] [Related]
10. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping. Veldman T; Vignon C; Schröck E; Rowley JD; Ried T Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389 [TBL] [Abstract][Full Text] [Related]
11. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies. Spikes AS; Hegmann K; Smith JL; Shaffer LG Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595 [TBL] [Abstract][Full Text] [Related]
12. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q. Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155 [TBL] [Abstract][Full Text] [Related]
13. Human cytogenetics: trends and techniques. Porter IH Prog Clin Pathol; 1973; 5():19-48. PubMed ID: 4131375 [No Abstract] [Full Text] [Related]
14. Chromosomes as markers in human cancer. Sandberg AA Int Adv Surg Oncol; 1981; 4():311-36. PubMed ID: 7019095 [No Abstract] [Full Text] [Related]
15. Cytogenetics of heritability in cancer. Evans HJ IARC Sci Publ; 1982; (39):35-56. PubMed ID: 6295935 [TBL] [Abstract][Full Text] [Related]
16. [Indications of chromosome and DNA analysis for the diagnosis of genetic diseases]. Romana SP; Gérard B Rev Prat; 1997 Jun; 47(11):1241-52. PubMed ID: 9238821 [No Abstract] [Full Text] [Related]
17. Human chromosomes karyotyping and their banding patterns. Seng CT J Singapore Paediatr Soc; 1977 Jun; 19(2):109-18. PubMed ID: 72190 [No Abstract] [Full Text] [Related]
19. Complex familial rearrangement of chromosome 9p24.3 detected by FISH. Repetto GM; Wagstaff J; Korf BR; Knoll JH Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094 [TBL] [Abstract][Full Text] [Related]
20. Analysis of banding patterns in a case of ring chromosome 21. Richer CL; Fitch N; Sitahal S; Murer-Orlando M; Jean P Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027 [No Abstract] [Full Text] [Related] [Next] [New Search]