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4. Characterisation of a 19-year-old "long-term survivor" with Edwards syndrome. Petek E; Pertl B; Tschernigg M; Bauer M; Mayr J; Wagner K; Kroisel PM Genet Couns; 2003; 14(2):239-44. PubMed ID: 12872820 [TBL] [Abstract][Full Text] [Related]
5. [Edwards syndrome--most frequent indications for genetic amniocentesis. Analysis of the last 5 years]. Chuchracki M; Janiak J; Ziółkowska K; Sedziak A; Opala T Przegl Lek; 2012; 69(10):1007-10. PubMed ID: 23421080 [TBL] [Abstract][Full Text] [Related]
6. Trisomy 18-Edwards syndrome: a report of three patients. Ejiwumni AB; Msamati BC Cent Afr J Med; 1993 May; 39(5):105-9. PubMed ID: 8131193 [No Abstract] [Full Text] [Related]
7. Unusual clinical history of a male infant with Edwards syndrome. Surányi A; Bitó T; Vajda G; Kaiser L; Gáspár G; Katona M; Szabó J; Pál A Pathol Oncol Res; 2009 Mar; 15(1):147-52. PubMed ID: 18575830 [TBL] [Abstract][Full Text] [Related]
8. [Fetal atrioventricular septal defect associated with Patau and Edwards syndromes, as well as trisomy 22]. Cesko I; Hajdú J; Marton T; Tóth-Pál E; Papp C; Papp Z Orv Hetil; 1998 May; 139(18):1087-9. PubMed ID: 9608772 [TBL] [Abstract][Full Text] [Related]
9. Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome). Nöthen MM; Eggermann T; Erdmann J; Eiben B; Hofmann D; Propping P; Schwanitz G Hum Genet; 1993 Oct; 92(4):347-9. PubMed ID: 8225314 [TBL] [Abstract][Full Text] [Related]
10. A patient with Edwards syndrome caused by a rare pseudodicentric chromosome 18 of paternal origin. Gravholt CH; Bugge M; Strømkjaer H; Caprani M; Henriques U; Petersen MB; Brandt CA Clin Genet; 1997 Jul; 52(1):56-60. PubMed ID: 9272714 [TBL] [Abstract][Full Text] [Related]
11. Trisomy 18 syndrome with congenital fibrotic change in the liver. Maruyama K; Koizumi T; Hirato J Pediatr Int; 2006 Dec; 48(6):646-7. PubMed ID: 17168992 [No Abstract] [Full Text] [Related]
12. [Trisomy 18 or Edwards' syndrome. A report of 4 clinical cases]. Giaccardi A; Sardi R; Priora U; Vivalda M; Domeneghetti G; Girone P Minerva Pediatr; 1991 Apr; 43(4):343-9. PubMed ID: 1870543 [TBL] [Abstract][Full Text] [Related]
13. Precocious puberty associated with partial trisomy 18q and monosomy 11q. Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872 [TBL] [Abstract][Full Text] [Related]
14. Double trisomy (48,XXX, +18). Tsukahara M; Fukuda M; Furukawa S; Kondoh O Am J Med Genet; 1994 Aug; 52(2):244. PubMed ID: 7802021 [No Abstract] [Full Text] [Related]
15. Prenatal detection of heart defects as an indication for chromosome analysis. Schwanitz G; Zerres K; Gembruch U; Bald R; Gamerdinger F; Hansmann M Ann Genet; 1990; 33(2):79-83. PubMed ID: 2146918 [TBL] [Abstract][Full Text] [Related]