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3. Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome. de France HF; Beemer FA; Senders RC; Schaminée-Main SC Clin Genet; 1985 Jan; 27(1):92-6. PubMed ID: 3978842 [TBL] [Abstract][Full Text] [Related]
4. Dermatoglyphics in trisomy 8 mosaicism. Schaumann B Humangenetik; 1974; 24(3):201-5. PubMed ID: 4442867 [No Abstract] [Full Text] [Related]
5. Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence. Graham DA; Jewitt MM; Fitzgerald PH Clin Genet; 1992 Jan; 41(1):36-8. PubMed ID: 1633645 [TBL] [Abstract][Full Text] [Related]
6. Trisomy 22 mosaicism with normal blood chromosomes. Case report with literature review. Lessick ML; Szego K; Wong PW Clin Pediatr (Phila); 1988 Sep; 27(9):451-4. PubMed ID: 3046809 [TBL] [Abstract][Full Text] [Related]
7. Trisomy 8 mosaicism. A case report and a proposed list of the clinical features. Kosztolànyi G; Bühler EM; Elmiger P; Stalder GR Eur J Pediatr; 1976 Nov; 123(4):293-300. PubMed ID: 991875 [TBL] [Abstract][Full Text] [Related]
8. Problems of detecting mosaicism in skin. A case of trisomy 8 mosaicism illustrating the advantages of in situ tissue culture. Procter SE; Watt JL; Lloyd DJ; Duffty P Clin Genet; 1984 Mar; 25(3):273-7. PubMed ID: 6705260 [TBL] [Abstract][Full Text] [Related]
9. Trisomy 8: an international study of 70 patients. Riccardi VM Birth Defects Orig Artic Ser; 1977; 13(3C):171-84. PubMed ID: 890109 [TBL] [Abstract][Full Text] [Related]
12. Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata. Wertelecki W; Breg WR; Graham JM; Iinuma K; Puck SM; Sergovich FR Am J Med Genet; 1986 Mar; 23(3):739-49. PubMed ID: 3953673 [TBL] [Abstract][Full Text] [Related]
13. Trisomy-8 mosaicism: report of a case. Silengo MC; Davi G; Crua G; Franceschini P Hum Genet; 1978 Jun; 42(3):323-6. PubMed ID: 669713 [TBL] [Abstract][Full Text] [Related]
14. First report of mosaic trisomy 12 in a liveborn individual. Patil SR; Bosch EP; Hanson JW Am J Med Genet; 1983 Mar; 14(3):453-60. PubMed ID: 6859097 [TBL] [Abstract][Full Text] [Related]
15. Trisomy 18 mosaicism: clues to the diagnosis. Bass HN; Fox M; Wulfsberg E; Sparkes RS; Crandall BF Clin Genet; 1982 Dec; 22(6):327-30. PubMed ID: 7160104 [TBL] [Abstract][Full Text] [Related]
16. Mosaic trisomy 9 syndrome with unusual phenotype. Kaminker CP; Daín L; Lamas MA; Sánchez JM Am J Med Genet; 1985 Oct; 22(2):237-41. PubMed ID: 3931476 [TBL] [Abstract][Full Text] [Related]
17. Pure trisomy 17p in 60% cells. Shabtai F; Shalev A; Chemke J; Halbrecht I; Elian E Hum Genet; 1979; 52(3):263-8. PubMed ID: 535886 [TBL] [Abstract][Full Text] [Related]
18. [Extreme tissue mosaicism in trisomy 8 syndrome. Trisomy 8 in fibroblasts and normal karyotype in lymphocytes]. Meisel-Stosiek M; Pfeiffer RA; Tietze HU Klin Padiatr; 1983; 195(5):365-8. PubMed ID: 6632718 [TBL] [Abstract][Full Text] [Related]
19. Trisomy 9 mosaicism syndrome. A case report and review of the literature. Tarani L; Colloridi F; Raguso G; Rizzuti A; Bruni L; Tozzi MC; Palermo D; Panero A; Vignetti P Ann Genet; 1994; 37(1):14-20. PubMed ID: 8010707 [TBL] [Abstract][Full Text] [Related]