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4. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements. Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734 [TBL] [Abstract][Full Text] [Related]
5. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q). Mercier S; Fellmann F; Cattin J; Bresson JL Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640 [TBL] [Abstract][Full Text] [Related]
6. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ]. Balícek P; Jüttnerová V; Jarosová M; Fialová J; Fiedler Z; Kolmanová J Cas Lek Cesk; 2001 Mar; 140(4):122-4. PubMed ID: 11284430 [TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findings. Aslan H; Karaman B; Yildirim G; Ceylan Y Prenat Diagn; 2005 Nov; 25(11):1024-7. PubMed ID: 16231308 [TBL] [Abstract][Full Text] [Related]
8. Fetal anomalies associated with an inversion duplication 13 chromosome. Rijhsinghani AG; Hruban RH; Stetten G Obstet Gynecol; 1988 Jun; 71(6 Pt 2):991-4. PubMed ID: 3287254 [TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of 13q-syndrome in a fetus with Dandy-Walker malformation. Gul A; Cebeci A; Erol O; Ceylan Y; Basaran S; Yuksel A Obstet Gynecol; 2005 May; 105(5 Pt 2):1227-9. PubMed ID: 15863591 [TBL] [Abstract][Full Text] [Related]
10. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement. Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779 [TBL] [Abstract][Full Text] [Related]
11. Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult. Papenhausen PR; Mueller OT; Johnson VP; Sutcliffe M; Diamond TM; Kousseff BG Am J Med Genet; 1995 Nov; 59(3):271-5. PubMed ID: 8599348 [TBL] [Abstract][Full Text] [Related]
12. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism. Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419 [TBL] [Abstract][Full Text] [Related]
18. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies. Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085 [TBL] [Abstract][Full Text] [Related]
19. Robertsonian translocations and abnormal phenotypes. Groupe de Cytogénéticiens Français. Ann Genet; 1989; 32(1):5-9. PubMed ID: 2665630 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis and management of congenital heart defect: significance of associated fetal anomalies and prenatal chromosome studies. Wladimiroff JW; Stewart PA; Sachs ES; Niermeijer MF Am J Med Genet; 1985 Jun; 21(2):285-90. PubMed ID: 3893127 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]