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22. Segregation patterns and phenotypes of unbalanced offspring in a large family with (10;18) chromosome translocation. Bernstein R; Pinto MR; Kromberg J; Wagner J; Jenkins T Am J Med Genet; 1985 Dec; 22(4):727-42. PubMed ID: 4073123 [TBL] [Abstract][Full Text] [Related]
23. Chromosome aberrations in 50 patients with idiopathic mental retardation and in 50 control subjects. Madison blind study 3. Daly RF J Pediatr; 1970 Sep; 77(3):444-53. PubMed ID: 5502094 [No Abstract] [Full Text] [Related]
24. [Deletion of the short arm of chromosome 18 and paternal mosaicism]. Laurent C; Michel M; Philippe N; Pinçon JA Ann Genet; 1970 Mar; 13(1):56-60. PubMed ID: 5311121 [No Abstract] [Full Text] [Related]
25. Partial trisomy 8 mosaicism with 46,XX/46,XX-8,+dic(8). Ray M; Hunter AG Ann Genet; 1980; 23(2):100-2. PubMed ID: 6967279 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Double autosomal trisomy and mosaicism for chromosomes no. 8 and no. 21. Wilson MG; Fujimoto A; Alfi OS J Med Genet; 1974 Mar; 11(1):96-101. PubMed ID: 4134622 [TBL] [Abstract][Full Text] [Related]
28. [The effect of mitomycin C on the chromosomes in cultured human cells]. Sinkus AG Tsitologiia; 1969 Aug; 11(8):933-40. PubMed ID: 5367201 [No Abstract] [Full Text] [Related]
29. Non-random occurrence of 7-14 translocations in human lymphocyte cultures. Welch JP; Lee CL; Beatty-DeSana JW; Hoggard MJ; Cooledge JW; Hecht F; McCaw BK; Peakman D; Robinson A Nature; 1975 May; 255(5505):241-5. PubMed ID: 1143322 [No Abstract] [Full Text] [Related]
30. Multiple chromosome aberrations: XO-XY-XYY mosaicism and a translocation in the same family. Ferrier PE; Ferrier SA; Schärer KO; Genton N; Hedinger C; Klein D Helv Paediatr Acta; 1967 Dec; 22(6):516-28. PubMed ID: 5592961 [No Abstract] [Full Text] [Related]
31. [Cytogenetic analysis of exudate cells in ovarian cancer]. Genes IS Tsitologiia; 1972 Jul; 14(7):890-5. PubMed ID: 4637822 [No Abstract] [Full Text] [Related]
32. Ring-18 and isopseudodicentric-18 in the same child: a hypothesis to account for common origin. Madan K; Vlasveld L; Barth PG Ann Genet; 1981; 24(1):12-6. PubMed ID: 6971609 [TBL] [Abstract][Full Text] [Related]
33. Autosomal chromosome aberrations. A review of the clinical syndromes caused by structural chromosome aberrations, mosaic-trisomies 8 and 9, and triploidy. Schinzel A Ergeb Inn Med Kinderheilkd; 1976; 38():37-94. PubMed ID: 782877 [No Abstract] [Full Text] [Related]
34. Guide to human chromosome defects. Redding A; Hirshhorn K Birth Defects Orig Artic Ser; 1970 May; 6(1):91-106. PubMed ID: 5522728 [No Abstract] [Full Text] [Related]
36. [Cytogenetic effect of n-nitroso-n-methylurea in the primary culture of fibroblast-like cells of human embryo]. Seleznev IuV Tsitologiia; 1968 Jun; 10(6):722-32. PubMed ID: 5708716 [No Abstract] [Full Text] [Related]
37. [Cytophysiologic and karyologic characteristics of reticular cell cultures sensitive and resistant to the cytopathic effect of enteroviruses]. Khesin IaE; Amchenkova AM; Karazhas NV; Gulevich NE Tsitologiia; 1972 Nov; 14(11):1382-91. PubMed ID: 4347505 [No Abstract] [Full Text] [Related]
38. Pachytene analysis in a human reciprocal (10;11) translocation. Ferguson-Smith MA; Page BM J Med Genet; 1973 Sep; 10(3):282-7. PubMed ID: 4774538 [TBL] [Abstract][Full Text] [Related]
39. Mitotic and meiotic studies of a familial reciprocal translocation between autosomes 15 and 18 in man. Fredga K; Rayner S Hereditas; 1967; 58(3):303-24. PubMed ID: 5584142 [No Abstract] [Full Text] [Related]