These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism. Faivre L; Viot G; Prieur M; Turleau C; Gosset P; Romana S; Munnich A; Vekemans M; Cormier-Daire V Am J Med Genet; 2000 Apr; 91(4):273-6. PubMed ID: 10766982 [TBL] [Abstract][Full Text] [Related]
4. [Free trisomy C, homogenous and with mosaicism]. Saint-Rome G; Gagnon J; Jeliu G; Duhaime M Union Med Can; 1972 Oct; 101(10):2121-9. PubMed ID: 4642700 [No Abstract] [Full Text] [Related]
5. Variable clinical expression of mosaic trisomy 16 in the newborn infant. Devi AS; Velinov M; Kamath MV; Eisenfeld L; Neu R; Ciarleglio L; Greenstein R; Benn P Am J Med Genet; 1993 Aug; 47(2):294-8. PubMed ID: 8213923 [TBL] [Abstract][Full Text] [Related]
6. Developmental and other pathologic changes in syndromes caused by chromosome abnormalities. Gilbert EF; Opitz JM Perspect Pediatr Pathol; 1982; 7():1-63. PubMed ID: 6214761 [No Abstract] [Full Text] [Related]
7. A specific phenotype associated with trisomy 15 mosaicism. Fryns JP; Kleczkowska A; Lagae L; Kenis H; van den Berghe H Ann Genet; 1993; 36(2):129-31. PubMed ID: 8215220 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Trisomy 2 mosaicism with caudal dysgenesis, Hirschsprung disease, and micro-anophthalmia. Prontera P; Stangoni G; Ardisia C; Rogaia D; Mencarelli A; Donti E Am J Med Genet A; 2011 Apr; 155A(4):928-30. PubMed ID: 21416586 [No Abstract] [Full Text] [Related]
15. Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome. Wilson GN; Barr M J Craniofac Genet Dev Biol; 1983; 3(4):313-6. PubMed ID: 6662905 [TBL] [Abstract][Full Text] [Related]
16. Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture. Harrison K; Eisenger K; Anyane-Yeboa K; Brown S Am J Med Genet; 1995 Aug; 58(2):147-51. PubMed ID: 8533806 [TBL] [Abstract][Full Text] [Related]