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.
4. Prenatal diagnosis of mosaic complete trisomy 1q. Schmitt CL; Moldenhauer JS; Wolfe H; Kaiser-Rogers K; Powell CM Am J Med Genet A; 2009 Aug; 149A(8):1801-5. PubMed ID: 19610082 [No Abstract] [Full Text] [Related]
5. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p. Leichtman LG; Zackowski JL; Storto PD; Newlin A Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648 [TBL] [Abstract][Full Text] [Related]
6. RSH (Smith-Lemli-Opitz) syndrome: "severe" phenotype with ectrodactyly. de Jong G; Kirby PA; Muller LM Am J Med Genet; 1998 Jan; 75(3):283-7. PubMed ID: 9475598 [TBL] [Abstract][Full Text] [Related]
8. Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father. De Smet L; Devriendt K; Fryns JP Genet Couns; 2001; 12(3):251-4. PubMed ID: 11693788 [TBL] [Abstract][Full Text] [Related]
9. Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases. Cassina M; Calò A; Salviati L; Alghisi A; Montaldi A; Clementi M Eur J Obstet Gynecol Reprod Biol; 2018 Feb; 221():23-27. PubMed ID: 29232625 [TBL] [Abstract][Full Text] [Related]
10. Mosaic partial trisomy 17q2. King PA; Ghosh A; Tang M J Med Genet; 1991 Sep; 28(9):641-3. PubMed ID: 1956067 [TBL] [Abstract][Full Text] [Related]
11. Acro-cardio-facial syndrome: a microdeletion syndrome? Toschi B; Valetto A; Bertini V; Congregati C; Cantinotti M; Assanta N; Simi P Am J Med Genet A; 2012 Aug; 158A(8):1994-9. PubMed ID: 22740423 [TBL] [Abstract][Full Text] [Related]
12. Transposition of great arteries in an infant born after prenatal diagnosis of trisomy 20 mosaicism. Karaoguz MY; Pala E; Kula S; Karaer K; Kan D; Nas T; Tunaoglu S Genet Couns; 2007; 18(4):437-43. PubMed ID: 18286825 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of mosaicism for triploidy and trisomy 13. Phelan MC; Curtis Rogers R; Michaelis RC; Moore CL; Blackburn W Prenat Diagn; 2001 Jun; 21(6):457-60. PubMed ID: 11438949 [TBL] [Abstract][Full Text] [Related]
14. [Genetic analysis and prenatal diagnosis of two Chinese families with split hand foot malformation]. Wang H; Xie J; Chen W; Geng Q; Xu X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):280-4. PubMed ID: 24928002 [TBL] [Abstract][Full Text] [Related]
15. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4. Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408 [TBL] [Abstract][Full Text] [Related]
16. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype. Jenderny J; Caliebe A; Beyer C; Grote W J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656 [TBL] [Abstract][Full Text] [Related]
17. Trisomy 16 and trisomy 16 Mosaicism: a review. Benn P Am J Med Genet; 1998 Sep; 79(2):121-33. PubMed ID: 9741470 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin. Paulyson KJ; Sherer DM; Christian SL; Lewis KM; Ledbetter DH; Salafia CM; Meck JM Prenat Diagn; 1996 Nov; 16(11):1021-6. PubMed ID: 8953635 [TBL] [Abstract][Full Text] [Related]
19. The challenging trisomy 16: a case report. Kontomanolis EN; Lambropoulou M; Georgiadis A; Gramatikopoulou I; Deftereou TH; Galazios G Clin Exp Obstet Gynecol; 2012; 39(3):412-3. PubMed ID: 23157062 [TBL] [Abstract][Full Text] [Related]
20. Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve. Fryns JP; Moerman P Genet Couns; 1998; 9(1):59-60. PubMed ID: 9555591 [No Abstract] [Full Text] [Related] [Next] [New Search]