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Journal Abstract Search
183 related items for PubMed ID: 16152651
1. Complete trisomy 1q with mosaic Y;1 translocation: a recurrent aneuploidy presenting diagnostic dilemmas. Scheuerle A, Heller K, Elder F. Am J Med Genet A; 2005 Oct 01; 138A(2):166-70. PubMed ID: 16152651 [Abstract] [Full Text] [Related]
2. Prenatal detection of mosaic trisomy 1q due to an unbalanced translocation in one fetus of a twin pregnancy following in vitro fertilization: a postzygotic error. Zeng S, Patil SR, Yankowitz J. Am J Med Genet A; 2003 Aug 01; 120A(4):464-9. PubMed ID: 12884423 [Abstract] [Full Text] [Related]
3. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations. Karaoguz MY, Biri A, Pala E, Kan D, Poyraz A, Kurdoglu M, Percin EF. Genet Couns; 2006 Aug 01; 17(2):197-204. PubMed ID: 16970038 [Abstract] [Full Text] [Related]
4. Mosaic trisomy 1q: The longest surviving case. Patel C, Hardy G, Cox P, Bowdin S, McKeown C, Russell AB. Am J Med Genet A; 2009 Aug 01; 149A(8):1795-800. PubMed ID: 19610079 [Abstract] [Full Text] [Related]
5. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born. Fernández-Novoa MC, Vargas MT, Granell MR, Carreto P. Prenat Diagn; 2004 Jun 01; 24(6):414-7. PubMed ID: 15229838 [Abstract] [Full Text] [Related]
6. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization. DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM. Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748 [Abstract] [Full Text] [Related]
10. 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 01; 149A(8):1801-5. PubMed ID: 19610082 [No Abstract] [Full Text] [Related]
11. Further clinical delineation in trisomy 1q32 syndrome. Nuño-Arana I, González-García JR, García-Cruz D. Ann Genet; 2001 Aug 01; 44(4):175-7. PubMed ID: 11755100 [Abstract] [Full Text] [Related]
13. Postnatal confirmation of prenatally diagnosed trisomy 16 mosaicism in two phenotypically abnormal liveborns. Pletcher BA, Sanz MM, Schlessel JS, Kunaporn S, McKenna C, Bialer MG, Alonso ML, Zaslav AL, Brown WT, Ray JH. Prenat Diagn; 1994 Oct 01; 14(10):933-40. PubMed ID: 7899268 [Abstract] [Full Text] [Related]
14. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis. Chen CP, Chang SJ, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Pan CW, Wang W. Taiwan J Obstet Gynecol; 2016 Aug 01; 55(4):602-3. PubMed ID: 27590391 [Abstract] [Full Text] [Related]
16. A rare case of a mosaic unbalanced translocation after chorionic villous sampling. Jeelani R, Chelliah A, Rauch K, Soto E, Ebrahim S, Bahado-Singh R, Jones T. Birth; 2013 Jun 01; 40(2):103-6. PubMed ID: 24635464 [Abstract] [Full Text] [Related]
19. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours]. Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E. Z Geburtshilfe Neonatol; 1996 Jun 01; 200(5):186-90. PubMed ID: 9035828 [Abstract] [Full Text] [Related]