176 related articles for article (PubMed ID: 33751529)
1. [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]
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 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]
4. [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]
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. Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.
Chen CP; Wu FT; Pan YT; Wu PS; Wang W
Taiwan J Obstet Gynecol; 2024 Jan; 63(1):77-80. PubMed ID: 38216274
[TBL] [Abstract][Full Text] [Related]
7. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
[No Abstract] [Full Text] [Related]
8. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.
Chen CP; Chang SD; Wang TH; Wang LK; Tsai JD; Liu YP; Chern SR; Wu PS; Su JW; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2013 Dec; 52(4):551-7. PubMed ID: 24411042
[TBL] [Abstract][Full Text] [Related]
9. [Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome].
Lin S; Luo Y; Wu J; Chen B; Ji Y; Zhou Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):89-92. PubMed ID: 28186603
[TBL] [Abstract][Full Text] [Related]
10. [Prenatal ultrasonic characteristics and genetic analysis of fetuses with chromosome 22q11 microdeletion syndrome].
Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Huang H; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Sep; 38(9):853-856. PubMed ID: 34487529
[TBL] [Abstract][Full Text] [Related]
11. [Prenatal diagnosis and genetic analysis of three fetuses with duodenal atresia or stenosis].
Chen N; Zeng W; Gao X; Luo Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Dec; 40(12):1484-1488. PubMed ID: 37994128
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. [Prenatal ultrasonographic manifestations and genetic analysis of eight fetuses with 16p11.2 microdeletions].
Cai M; Huang H; Lin N; Su L; Wu X; Xie X; Li Y; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Feb; 39(2):227-230. PubMed ID: 35076926
[TBL] [Abstract][Full Text] [Related]
14. [Prenatal diagnosis of a fetus with Phelan-McDermid syndrome and 21q21 microdeletion by multiple genetic techniques].
Shen H; Li S; Jin Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1387-1390. PubMed ID: 33306829
[TBL] [Abstract][Full Text] [Related]
15. [Prenatal diagnosis of fetuses with renal anomalies by whole genome sequencing].
Qiao F; Hu P; Zhang C; Wang Y; Zhou R; Luo C; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Aug; 39(8):819-823. PubMed ID: 35929929
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Prenatal diagnosis and clinical analysis of two fetuses with Cat-eye syndrome].
Wu X; An G; He D; Shen Q; Cai M; Huang H; Lin Y; Xu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):498-501. PubMed ID: 31030443
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. [Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].
Ji X; Hu H; Wang Y; Liang D; Luo C; Meng L; Zhou J; Cao L; Ma D; Hu P; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):853-856. PubMed ID: 29188615
[TBL] [Abstract][Full Text] [Related]
20. [Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].
Li W; Fang R; Shen X; Yao J; Xue J; Shen G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1344-1348. PubMed ID: 33306818
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]