270 related articles for article (PubMed ID: 16231308)
1. 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]
2. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
Xu J; Chernos J; Roland B
Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of a fetus with partial trisomy 7p.
Ozgun MT; Batukan C; Basbug M; Akgun H; Caglayan O; Dundar M
Fetal Diagn Ther; 2007; 22(3):229-32. PubMed ID: 17228165
[TBL] [Abstract][Full Text] [Related]
6. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.
Peng HH; Wang TH; Hsueh DW; Chang SD; Soong YK
Prenat Diagn; 2005 Jun; 25(6):470-4. PubMed ID: 15966037
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.
Chen CP; Liu FF; Jan SW; Yang YC; Lan CC
Prenat Diagn; 1996 Dec; 16(12):1137-40. PubMed ID: 8994250
[TBL] [Abstract][Full Text] [Related]
11. Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).
Fryns JP; Kleczkowska A
Ann Genet; 1987; 30(2):109-10. PubMed ID: 3499841
[TBL] [Abstract][Full Text] [Related]
12. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
Wang H; McLaughlin M; Thompson C; Hunter AG
Am J Med Genet; 1993 Jun; 46(5):559-62. PubMed ID: 8322821
[TBL] [Abstract][Full Text] [Related]
13. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of a der(X)t(X;15)(p22.2;q11.2) inherited from a maternal translocation X;15.
Garcia-Heras J; Ulm JE; Shaver DE; Hall E; Saikevych IA
Prenat Diagn; 1998 Jul; 18(7):747-50. PubMed ID: 9706659
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of the distal 11q deletion and review of the literature.
Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Chen LF; Wang W
Prenat Diagn; 2004 Feb; 24(2):130-6. PubMed ID: 14974122
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
Pivnick EK; Wilroy RS; Summitt JB; Tucker B; Herrod HG; Tharapel AT
Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y; Yakut T; Egelí U; Ozerkan K
Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of partial trisomy through in situ hybridization on amniocytes with whole chromosome and centromere-specific DNA probes. A case report.
Blancato JK; Eglinton G; George J; Benkendorf J; Pinckert T; Meck J
J Reprod Med; 1995 Jul; 40(7):537-9. PubMed ID: 7473445
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
