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25. Cardiac and extra-cardiac anomalies as indicators for trisomies 13 and 18: a prenatal ultrasound study. Wladimiroff JW; Stewart PA; Reuss A; Sachs ES Prenat Diagn; 1989 Jul; 9(7):515-20. PubMed ID: 2671976 [TBL] [Abstract][Full Text] [Related]
26. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism. Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560 [TBL] [Abstract][Full Text] [Related]
27. A boy with severe manifestations of type A1 brachydactyly. Slavotinek A; Donnai D Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826 [TBL] [Abstract][Full Text] [Related]
28. Hands and feet in the Apert syndrome. Cohen MM; Kreiborg S Am J Med Genet; 1995 May; 57(1):82-96. PubMed ID: 7645606 [TBL] [Abstract][Full Text] [Related]
29. Prenatal confirmation of true fetal trisomy 22 mosaicism by fetal skin biopsy following normal fetal blood sampling. Berghella V; Wapner RJ; Yang-Feng T; Mahoney MJ Prenat Diagn; 1998 Apr; 18(4):384-9. PubMed ID: 9602487 [TBL] [Abstract][Full Text] [Related]
30. Normal outcome of a pregnancy with mosaicism for double trisomy in amniotic fluid cells. Bartels I; Franke U; Braulke I; Rauskolb R; Raab-Vetter M Prenat Diagn; 1997 Sep; 17(9):877-8. PubMed ID: 9316135 [TBL] [Abstract][Full Text] [Related]
31. Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review. Sun S; Zhan F; Jiang J; Zhang X; Yan L; Cai W; Liu H; Cao D BMC Med Genomics; 2019 Dec; 12(1):197. PubMed ID: 31864361 [TBL] [Abstract][Full Text] [Related]
32. Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13). Tschernigg M; Petek E; Leonhardtsberger A; Wagner K; Kroisel PM Genet Couns; 2002; 13(3):303-7. PubMed ID: 12416638 [TBL] [Abstract][Full Text] [Related]
33. A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature review. Hu X; Ayala SS; Dyer L; Guan Q; Pena L Am J Med Genet A; 2021 Jun; 185(6):1864-1869. PubMed ID: 33759348 [TBL] [Abstract][Full Text] [Related]
34. Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome. Petit F; Holder-Espinasse M; Duban-Bedu B; Bouquillon S; Boute-Benejean O; Bazin A; Rouland V; Manouvrier-Hanu S; Delobel B Clin Genet; 2012 Mar; 81(3):265-71. PubMed ID: 21204802 [TBL] [Abstract][Full Text] [Related]
37. On the significance of true trisomy 20 mosaicism in amniotic fluid culture. Djalali M; Steinbach P; Schwinger E; Schwanitz G; Tettenborn U; Wolf M Hum Genet; 1985; 69(4):321-6. PubMed ID: 3988281 [TBL] [Abstract][Full Text] [Related]
38. Trisomy 18 with unilateral atypical ectrodactyly. Rogers RC Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239 [No Abstract] [Full Text] [Related]
39. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition. Martin RA; Jones MC; Jones KL Am J Med Genet; 1993 Apr; 46(2):129-31. PubMed ID: 8387244 [No Abstract] [Full Text] [Related]
40. Prenatal diagnosis of low level trisomy 15 mosaicism: review of the literature. Zaslav AL; Fallet S; Brown S; Ebert R; Fleischer A; Valderama E; Fox JE Clin Genet; 1998 Apr; 53(4):286-92. PubMed ID: 9650767 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]