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4. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations. Wilson WG; Shires MA; Willson KA; Wyandt HE; Harris LM; Kelly TE Am J Med Genet; 1983 Sep; 16(1):131-6. PubMed ID: 6638063 [TBL] [Abstract][Full Text] [Related]
5. Double autosomal trisomy mosaicism: 47,XY,+21/48,XY,+13,+21. Barnett SH; Jhaveri M; Gertner M Am J Med Genet; 1987 Oct; 28(2):501-2. PubMed ID: 3425623 [No Abstract] [Full Text] [Related]
6. [18 ring chromosome. A clinical and cytopathogenetic study (author's transl)]. Carbone LD; Caffarena G; Arslanian A; Cresta E; de Filippi M; Frateschi M Pathologica; 1978; 70(1009-1010):687-92. PubMed ID: 755240 [No Abstract] [Full Text] [Related]
7. Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature. Kaplan LC; Wayne A; Crowell S; Latt SA Am J Med Genet; 1986 Apr; 23(4):925-30. PubMed ID: 3515939 [TBL] [Abstract][Full Text] [Related]
8. [Syndrome of multiple abnormalities in a child with mosaicism 46, XY/47, XY, +E]. Balcar-Boroń A; Sawa H; Slowik J; Marcinkowska A; Robińska E Pediatr Pol; 1977 Oct; 52(10):1161-4. PubMed ID: 583678 [No Abstract] [Full Text] [Related]
9. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example. Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064 [TBL] [Abstract][Full Text] [Related]
10. [Clinical and cytogenetic considerations on a case of monosomy 21 in (45, XX-21/46,XY) mosaicism]. Butnariu J; Olinici CD; Popescu A; Giurgiuman M Rev Pediatr Obstet Ginecol Pediatr; 1977; 26(4):331-6. PubMed ID: 414334 [No Abstract] [Full Text] [Related]
12. Unilateral microtia in an infant with trisomy 18 mosaicism. Giannatou E; Leze H; Katana A; Kolialexi A; Mavrou A; Kanavakis E; Kitsiou-Tzeli S Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416 [TBL] [Abstract][Full Text] [Related]
13. Histopathology and molecular cytogenetics of a corneal opacity associated with the trisomy 8 mosaic syndrome (46,XY/47,XY, +8). Scott JA; Howard PJ; Smith PA; Fryer A; Easty DL; Patterson A; Kaye SB Cornea; 1997 Jan; 16(1):35-41. PubMed ID: 8985632 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant. Milunsky JM; Wyandt HE; Huang XL; Kang XZ; Elias ER; Milunsky A Am J Med Genet; 1996 Jan; 61(3):269-73. PubMed ID: 8741873 [TBL] [Abstract][Full Text] [Related]