163 related articles for article (PubMed ID: 31400135)
1. [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]
2. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
[TBL] [Abstract][Full Text] [Related]
5. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.
Chen CP; Su YN; Young RS; Tsai FJ; Wu PC; Chern SR; Town DD; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):506-12. PubMed ID: 21199755
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Diagnosis of a fetus with partial 17p trisomy using chromosomal microarray analysis].
Zhao L; Wan B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):488-490. PubMed ID: 31030440
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia.
Jung SH; Shim SH; Park SH; Park JE; Park HR; Ahn EH; Kim SH; Cha DH
Gene; 2012 May; 498(2):237-41. PubMed ID: 22366303
[TBL] [Abstract][Full Text] [Related]
9. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
Shi S; Pan G; Yang Y; Yan R; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
[TBL] [Abstract][Full Text] [Related]
12. [Application of chromosomal karyotyping analysis and array CGH for fetal abnormalities detected by ultrasonography].
Wang Y; Tang B; Guo L; Chen H; Lu J; Yin A
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):550-553. PubMed ID: 28777857
[TBL] [Abstract][Full Text] [Related]
13. [Diagnosis of a fetus with a de novo 16q partial trisomy syndrome].
Hu L; Wang W; Li H; Zhou S; Liu S; Yang M; Bu X; He J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1084-1086. PubMed ID: 32924106
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).
Chen CP; Hung FY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2016 Apr; 55(2):288-92. PubMed ID: 27125417
[TBL] [Abstract][Full Text] [Related]
15. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Applied research of combined G-banding and array-CGH in the prenatal diagnosis of ultrasonographic abnormalities in fetuses].
Fu W; Lu J; Xu L; Zheng L; Zhang Y; Zhong Y; Wang Y; Jin Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):737-42. PubMed ID: 25449078
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly.
Sung PL; Chang CM; Chen CY; Wang PH; Chao KC; Wen KC; Cheng YY; Li YC; Lin CC
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):260-5. PubMed ID: 22795105
[TBL] [Abstract][Full Text] [Related]
19. Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid.
Miura S; Miura K; Masuzaki H; Miyake N; Yoshiura KI; Sosonkina N; Harada N; Shimokawa O; Nakayama D; Yoshimura S; Matsumoto N; Niikawa N; Ishimaru T
J Hum Genet; 2006; 51(5):412-417. PubMed ID: 16622586
[TBL] [Abstract][Full Text] [Related]
20. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
