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6. Antepartum diagnosis of arthrogryposis associated with trisomy 18. Kopelman JN Mil Med; 1993 Jul; 158(7):498-9. PubMed ID: 8351055 [TBL] [Abstract][Full Text] [Related]
7. Fetal pyelectasis: does fetal gender modify the risk of major trisomies? Bornstein E; Barnhard Y; Donnenfeld A; Ferber A; Divon MY Obstet Gynecol; 2006 Apr; 107(4):877-9. PubMed ID: 16582126 [TBL] [Abstract][Full Text] [Related]
8. The etiology of arthrogryposis (multiple congenital contracture). Swinyard CA; Bleck EE Clin Orthop Relat Res; 1985 Apr; (194):15-29. PubMed ID: 3884205 [TBL] [Abstract][Full Text] [Related]
9. Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy. Chen CP; Chang TY; Lin HH; Chern SR; Wang W Taiwan J Obstet Gynecol; 2008 Mar; 47(1):93-4. PubMed ID: 18400591 [No Abstract] [Full Text] [Related]
10. Effect of fetal diagnosis on the outcomes of second-trimester pregnancy termination for fetal abnormalities: a pilot study. Lo TK; Lau WL; Lai FK; Lam HS; Tse HY; Leung WC; Chin RK J Matern Fetal Neonatal Med; 2008 Aug; 21(8):523-7. PubMed ID: 18609362 [TBL] [Abstract][Full Text] [Related]
11. [20 cases of trisomy 18. Sex-ratio in relation to age of the mother]. Le Marec BM; Lair JC; Kérisit J; Le Mée F; Sénécal J Ann Pediatr (Paris); 1977 Feb; 24(2):125-36. PubMed ID: 16211953 [No Abstract] [Full Text] [Related]
13. Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter). Chen CP; Chern SR; Chang TY; Lee CC; Chen WL; Wang W Prenat Diagn; 2005 Nov; 25(11):1069-71. PubMed ID: 16302165 [No Abstract] [Full Text] [Related]
14. First trimester diagnosis of iniencephaly associated with fetal malformations and trisomy 18: report of a new case and gene analysis on folate metabolism in parents. Tonni G; Azzoni D; Panteghini M; Ventura A; Cavalli P Congenit Anom (Kyoto); 2007 Sep; 47(3):101-4. PubMed ID: 17688469 [TBL] [Abstract][Full Text] [Related]
15. [Fetal pathology within the scope of prenatal diagnosis]. Rehder H Verh Dtsch Ges Pathol; 1982; 66():58-74. PubMed ID: 7184273 [No Abstract] [Full Text] [Related]
16. Arthrogryposis multiplex congenita: twenty-three cases in an Arab kindred. Lebenthal E; Shochet SB; Adam A; Seelenfreund M; Fried A; Najenson T; Sandbank U; Matoth Y Pediatrics; 1970 Dec; 46(6):891-9. PubMed ID: 5491443 [No Abstract] [Full Text] [Related]
17. Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisis. Donaldson SJ; Wright CA; de Ravel TJ Prenat Diagn; 1999 Jun; 19(6):580-2. PubMed ID: 10416978 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of pure distal 18q deletion. Chen CP; Chern SR; Hung FY; Hsu CY; Chang TY; Lee CC; Town DD; Chen WL; Chen LF; Tzen CY; Wang W; Ma R Prenat Diagn; 2006 Feb; 26(2):184-5. PubMed ID: 16470512 [No Abstract] [Full Text] [Related]
19. Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs. Chen CP; Weng SS; Chern SR; Chen SW; Wu FT; Wang W Taiwan J Obstet Gynecol; 2021 May; 60(3):549-550. PubMed ID: 33966746 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of monosomy 4p14-->pter and trisomy 11q25-->qter: clinical presentations and outcomes. Peng HH; Wang TH; Chao AS; Chang YL; Chang SD; Soong YK Prenat Diagn; 2005 Dec; 25(12):1133-7. PubMed ID: 16231301 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]