190 related articles for article (PubMed ID: 26137780)
1. [PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN].
Stoyanova V; Nedeva N; Linev A; Ivanov H; Petrova P; Krushkov K; Stratieva V; Vachev T
Akush Ginekol (Sofiia); 2015; 54(3):43-7. PubMed ID: 26137780
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Prenatal diagnosis of der(11)t(11;18)(q24;q21.3) due to paternal balanced translocation and both parents are carriers of alpha-thalassemia-1--a case report.
Chao MC; Yang SY; Chang Y; Huang YW; Liu TC; Lee JP; Chen BH
Kaohsiung J Med Sci; 2001 Aug; 17(8):430-6. PubMed ID: 11715843
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
6. [Prenatal diagnosis of partial trisomy 3q in a fetus].
Su N; Lou G; Wang H; Hao B; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):813-816. PubMed ID: 31400135
[TBL] [Abstract][Full Text] [Related]
7. [Prenatal diagnosis of a fetus with partial trisomy 8p resulting from a balanced maternal translocation by array-based comparative genomic hybridization].
Guo C; Wang J; Zhao L; Liu J; Wang J; Xiao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):375-7. PubMed ID: 26037354
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Chen CP; Chern SR; Lee CC; Chen LF; Chin DT; Tzen CY; Wang W
Prenat Diagn; 2003 Sep; 23(9):758-61. PubMed ID: 12975789
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.
Chen CP; Chang YL; Chern SR; Wu PS; Su JW; Chen WL; Chen LF; Wang W
Gene; 2013 Mar; 516(1):132-7. PubMed ID: 23266805
[TBL] [Abstract][Full Text] [Related]
10. A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9).
Hengstschläger M; Bettelheim D; Repa C; Lang S; Deutinger J; Bernaschek G
Fetal Diagn Ther; 2002; 17(4):243-6. PubMed ID: 12065954
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature.
Li L; Zhang X; Shi Q; Li L; Jiang Y; Liu R; Zhang H
J Clin Lab Anal; 2021 Jan; 35(1):e23582. PubMed ID: 32951212
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report.
Ali TM; Mateu-Brull E; Balaguer N; Dantas C; Borges HR; de Oliveira MQG; Rodrigo L; Campos-Galindo I; Navarro R; Milán M
Eur J Med Res; 2021 Jun; 26(1):64. PubMed ID: 34187576
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prenatal identification of partial 3q duplication syndrome.
Pasińska M; Adamczak R; Repczyńska A; Łazarczyk E; Iskra B; Runge AK; Haus O
BMC Med Genomics; 2019 Jun; 12(1):85. PubMed ID: 31196198
[TBL] [Abstract][Full Text] [Related]
19. Characterization of a balanced complex chromosomal rearrangement carrier ascertained through a fetus with dup15q26.3 and del5p15.33: case report.
Lledo B; Ortiz JA; Morales R; Manchon I; Galan F; Bernabeu A; Bernabeu R
Hum Fertil (Camb); 2013 Sep; 16(3):215-7. PubMed ID: 23905868
[TBL] [Abstract][Full Text] [Related]
20. Parental balanced chromosomal rearrangement leading to major genomic imbalance and an autosomal trisomy resulting in consecutive pregnancy loss: a case report.
Shrivastava A; Thakur S; Nath T; Debnath AVF; Bakshi SR
J Genet; 2021; 100():. PubMed ID: 34344842
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
