157 related articles for article (PubMed ID: 36184103)
1. [Prenatal diagnosis of two fetuses with 17q12 microdeletion syndrome].
Wang X; Xu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Oct; 39(10):1153-1157. PubMed ID: 36184103
[TBL] [Abstract][Full Text] [Related]
2. Prenatal ultrasound features and genetic analysis for 17q12 microdeletion syndrome.
Zhang Z; Pan L; Chen K; Tan R
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2021 Dec; 46(12):1370-1374. PubMed ID: 35232906
[TBL] [Abstract][Full Text] [Related]
3. [Prenatal diagnosis of 17q12 microdeletion syndrome in fetal renal abnormalities].
Jiang YL; Qi QW; Zhou XY; Geng FF; Bai JJ; Hao N; Liu JT
Zhonghua Fu Chan Ke Za Zhi; 2017 Oct; 52(10):662-668. PubMed ID: 29060963
[No Abstract] [Full Text] [Related]
4. [Ultrasonographic phenotype and genetic analysis of fetuses with 17q12 microdeletion].
Cai M; Huang H; Su L; Wu X; Xie X; Li Y; Lin N; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Dec; 39(12):1329-1333. PubMed ID: 36453953
[TBL] [Abstract][Full Text] [Related]
5. [Clinical and genetic analysis of a fetus with 17q12 microdeletion syndrome].
Lyu Y; Lin M; Shao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun; 40(6):737-743. PubMed ID: 37212013
[TBL] [Abstract][Full Text] [Related]
6. Classifying and evaluating fetuses with multicystic dysplastic kidney in etiologic studies.
Cai M; Guo C; Wang X; Lin M; Xu S; Huang H; Lin N; Xu L
Exp Biol Med (Maywood); 2023 May; 248(10):858-865. PubMed ID: 37208928
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities.
Wan S; Zheng Y; Dang Y; Song T; Chen B; Zhang J
Mol Cytogenet; 2019; 12():19. PubMed ID: 31131025
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of fetal multicystic dysplastic kidney via high-resolution whole-genome array.
Fu F; Chen F; Li R; Zhang Y; Pan M; Li D; Liao C
Nephrol Dial Transplant; 2016 Oct; 31(10):1693-8. PubMed ID: 26932690
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
Mademont-Soler I; Morales C; Soler A; Martínez-Crespo JM; Shen Y; Margarit E; Clusellas N; Obón M; Wu BL; Sánchez A
Ultrasound Obstet Gynecol; 2013 Apr; 41(4):375-82. PubMed ID: 23233332
[TBL] [Abstract][Full Text] [Related]
10. Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome.
Cai M; Lin M; Guo N; Fu M; Xu L; Lin N; Huang H
Front Pediatr; 2022; 10():910497. PubMed ID: 36034547
[TBL] [Abstract][Full Text] [Related]
11. Prenatal Diagnosis and Molecular Cytogenetic Analyses of a Rare 17q12 Microdeletion and Microduplication in a Family with a Normal Phenotype.
Xie M; Tang D; Guo F
Altern Ther Health Med; 2024 Jan; ():. PubMed ID: 38330560
[TBL] [Abstract][Full Text] [Related]
12. [Prenatal genetic diagnosis of the fetuses with isolated corpus callosum abnormality].
She Q; Zhen L; Fu F; Lei TY; Li LS; Li R; Wang D; Zhang YL; Jing XY; Yi CX; Zhong HZ; Tan WH; Li FG; Liao C
Zhonghua Fu Chan Ke Za Zhi; 2022 Sep; 57(9):671-677. PubMed ID: 36177578
[No Abstract] [Full Text] [Related]
13. Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series.
Zhou CX; Zhu XY; Zhu YJ; Gu LL; He LL; Liu W; Yang Y; Wu X; Duan HL; Ru T; Li J
Taiwan J Obstet Gynecol; 2021 Mar; 60(2):232-237. PubMed ID: 33678321
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis and family analysis of 17q12 microdeletion syndrome with fetal renal abnormalities.
Zhang F; Gu Q; Song J; Zhao Y; Wang Z; Men S; Wang L
Front Genet; 2024; 15():1401315. PubMed ID: 38957807
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies.
Li R; Fu F; Zhang YL; Li DZ; Liao C
Taiwan J Obstet Gynecol; 2014 Dec; 53(4):579-82. PubMed ID: 25510704
[TBL] [Abstract][Full Text] [Related]
16. [Prenatal diagnosis and genetic analysis of two fetuses with paternally derived 17q12 microdeletions].
Zhang Y; Liu Y; Yan L; Zhuang D; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):224-227. PubMed ID: 33751529
[TBL] [Abstract][Full Text] [Related]
17. [Application of chromosome microarray analysis for fetuses with multicystic dysplastic kidney].
Chen F; Lei T; Fu F; Li R; Zhang Y; Jing X; Yang X; Han J; Zhen L; Pan M; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):752-757. PubMed ID: 27984599
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism.
Gilboa Y; Perlman S; Pode-Shakked N; Pode-Shakked B; Shrim A; Azaria-Lahav E; Dekel B; Yonath H; Berkenstadt M; Achiron R
Prenat Diagn; 2016 Nov; 36(11):1027-1032. PubMed ID: 27634641
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of HNF1B-associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome?
Vasileiou G; Hoyer J; Thiel CT; Schaefer J; Zapke M; Krumbiegel M; Kraus C; Zweier M; Uebe S; Ekici AB; Schneider M; Wiesener M; Rauch A; Faschingbauer F; Reis A; Zweier C; Popp B
Prenat Diagn; 2019 Nov; 39(12):1136-1147. PubMed ID: 31498910
[TBL] [Abstract][Full Text] [Related]
20. [Genetic diagnosis of microcephaly].
Liao XF; Liao BJ; Tan WH; Wang L; Wang DD; Tang EF; Li FG; Pan XF; Ji LH; She Q
Zhonghua Fu Chan Ke Za Zhi; 2023 Mar; 58(3):178-184. PubMed ID: 36935194
[No Abstract] [Full Text] [Related]
[Next] [New Search]
