122 related articles for article (PubMed ID: 35711925)
1. The Evaluation of Genetic Diagnosis on High-Risk Fetal CAKUT.
Liu W; Shi X; Li Y; Qiao F; Chen S; Feng L; Zeng W; Deng D; Wu Y
Front Genet; 2022; 13():869525. PubMed ID: 35711925
[No Abstract] [Full Text] [Related]
2. Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Wu CW; Lim TY; Wang C; Seltzsam S; Zheng B; Schierbaum L; Schneider S; Mann N; Connaughton DM; Nakayama M; van der Ven AT; Dai R; Kolvenbach CM; Kause F; Ottlewski I; Stajic N; Soliman NA; Kari JA; El Desoky S; Fathy HM; Milosevic D; Turudic D; Al Saffar M; Awad HS; Eid LA; Ramanathan A; Senguttuvan P; Mane SM; Lee RS; Bauer SB; Lu W; Hilger AC; Tasic V; Shril S; Sanna-Cherchi S; Hildebrandt F
Eur Urol Open Sci; 2022 Oct; 44():106-112. PubMed ID: 36185583
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES).
Koenigbauer JT; Fangmann L; Reinhardt C; Weichert A; Henrich W; Saskia B; Gabriel HP
Arch Gynecol Obstet; 2024 Jun; 309(6):2613-2622. PubMed ID: 37535131
[TBL] [Abstract][Full Text] [Related]
4. Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract.
Lei TY; Fu F; Li R; Wang D; Wang RY; Jing XY; Deng Q; Li ZZ; Liu ZQ; Yang X; Li DZ; Liao C
Nephrol Dial Transplant; 2017 Oct; 32(10):1665-1675. PubMed ID: 28387813
[TBL] [Abstract][Full Text] [Related]
5. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Petrovski S; Aggarwal V; Giordano JL; Stosic M; Wou K; Bier L; Spiegel E; Brennan K; Stong N; Jobanputra V; Ren Z; Zhu X; Mebane C; Nahum O; Wang Q; Kamalakaran S; Malone C; Anyane-Yeboa K; Miller R; Levy B; Goldstein DB; Wapner RJ
Lancet; 2019 Feb; 393(10173):758-767. PubMed ID: 30712878
[TBL] [Abstract][Full Text] [Related]
6. [Analysis of 26 fetuses with congenital anomalies of the kidney and urinary tract by whole exome sequencing].
Lei T; Fu F; Li R; Wang D; Yang D; Wang F; Yang X; Pan M; Zhen L; Han J; Li D; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):856-859. PubMed ID: 30512163
[TBL] [Abstract][Full Text] [Related]
7. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing.
Zhou X; Wang Y; Shao B; Wang C; Hu P; Qiao F; Xu Z
J Clin Lab Anal; 2020 Nov; 34(11):e23480. PubMed ID: 32779812
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
Lei TY; Fu F; Li R; Yu QX; Du K; Zhang WW; Deng Q; Li LS; Wang D; Yang X; Zhen L; Li DZ; Liao C
Prenat Diagn; 2020 Sep; 40(10):1290-1299. PubMed ID: 32436246
[TBL] [Abstract][Full Text] [Related]
9. Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.
Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Chen X; Dai Y; Lin Y; Huang H; Xu L
J Clin Lab Anal; 2020 Jan; 34(1):e23025. PubMed ID: 31506986
[TBL] [Abstract][Full Text] [Related]
10. The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype.
He M; Du L; Xie H; Zhang L; Gu Y; Lei T; Zheng J; Chen D
Front Genet; 2021; 12():627204. PubMed ID: 34367232
[TBL] [Abstract][Full Text] [Related]
11. Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project.
Huang Z; Shen Q; Wu B; Wang H; Dong X; Lu Y; Cheng G; Wang L; Lu W; Chen L; Kang W; Li L; Pan X; Wei Q; Zhuang D; Chen D; Yin Z; Yang L; Ni Q; Liu R; Li G; Zhang P; Qian Y; Peng X; Wang Y; Cao Y; Xu H; Hu L; Yang L; Zhou W
Kidney Int Rep; 2023 Nov; 8(11):2376-2384. PubMed ID: 38025242
[TBL] [Abstract][Full Text] [Related]
12. Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Bekheirnia MR; Bekheirnia N; Bainbridge MN; Gu S; Coban Akdemir ZH; Gambin T; Janzen NK; Jhangiani SN; Muzny DM; Michael M; Brewer ED; Elenberg E; Kale AS; Riley AA; Swartz SJ; Scott DA; Yang Y; Srivaths PR; Wenderfer SE; Bodurtha J; Applegate CD; Velinov M; Myers A; Borovik L; Craigen WJ; Hanchard NA; Rosenfeld JA; Lewis RA; Gonzales ET; Gibbs RA; Belmont JW; Roth DR; Eng C; Braun MC; Lupski JR; Lamb DJ
Genet Med; 2017 Apr; 19(4):412-420. PubMed ID: 27657687
[TBL] [Abstract][Full Text] [Related]
13. Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis.
Li S; Han X; Wang Y; Chen S; Niu J; Qian Z; Li P; Jin L; Xu C
Prenat Diagn; 2019 Feb; 39(3):165-174. PubMed ID: 30650192
[TBL] [Abstract][Full Text] [Related]
14. Genetic testing and diagnostic strategies of fetal skeletal dysplasia: a preliminary study in Wuhan, China.
Liu W; Cao J; Shi X; Li Y; Qiao F; Wu Y
Orphanet J Rare Dis; 2023 Oct; 18(1):336. PubMed ID: 37875969
[TBL] [Abstract][Full Text] [Related]
15. Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
Monier I; Receveur A; Houfflin-Debarge V; Goua V; Castaigne V; Jouannic JM; Mousty E; Saliou AH; Bouchghoul H; Rousseau T; Valat AS; Groussolles M; Fuchs F; Benoist G; Degre S; Massardier J; Tsatsaris V; Kleinfinger P; Zeitlin J; Benachi A;
Am J Obstet Gynecol; 2021 Dec; 225(6):676.e1-676.e15. PubMed ID: 34058167
[TBL] [Abstract][Full Text] [Related]
16. Whole Exome Sequencing Analysis in Fetal Skeletal Dysplasia Detected by Ultrasonography: An Analysis of 38 Cases.
Peng Y; Yang S; Huang X; Pang J; Liu J; Hu J; Shen X; Tang C; Wang H
Front Genet; 2021; 12():728544. PubMed ID: 34567078
[No Abstract] [Full Text] [Related]
17. Copy number variations associated with fetal congenital kidney malformations.
Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Chen X; Lin Y; Huang H; Xu L
Mol Cytogenet; 2020; 13():11. PubMed ID: 32211073
[TBL] [Abstract][Full Text] [Related]
18. Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary Tract.
Harris M; Schuh MP; McKinney D; Kaufman K; Erkan E
Front Pediatr; 2022; 10():898773. PubMed ID: 35990004
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of fetal digestive system malformations and pregnancy outcomes at a tertiary referral center in Fujian, China: A retrospective study.
Liang B; Yang F; Huang H; Liu Z; Ji Q; Wang Y; Wu X; Lin Y; Xie L; Zhao W; Cao H; Xu L; Lin N
Heliyon; 2023 Nov; 9(11):e21546. PubMed ID: 38027951
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis and outcomes in fetuses with duplex kidney.
Ma C; Huang R; Fu F; Zhou H; Wang Y; Yan S; Guo F; Chen H; Li L; Jing X; Li F; Han J; Li D; Li R; Liao C
Int J Gynaecol Obstet; 2024 Jul; 166(1):353-359. PubMed ID: 38189110
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]