137 related articles for article (PubMed ID: 38330560)
1. 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]
2. 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]
3. 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]
4. 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]
5. Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene.
Luo M; Gu X; Zhou T; Chen C
Mol Cytogenet; 2022 Dec; 15(1):53. PubMed ID: 36544198
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2.
Li M; Liu L; Wu Y; Guan J
J Int Med Res; 2022 Jul; 50(7):3000605221109400. PubMed ID: 35808818
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series.
Jing XY; Huang LY; Zhen L; Han J; Li DZ
J Obstet Gynaecol; 2019 Apr; 39(3):323-327. PubMed ID: 30634886
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Prenatal diagnosis and genetic counseling of an inherited unbalanced chromosome abnormalities in a Chinese family.
Zhang Y; Chen J; Feng Z; Li W
Mol Cytogenet; 2022 Aug; 15(1):34. PubMed ID: 35971114
[TBL] [Abstract][Full Text] [Related]
12. The Prenatal Diagnosis of Seven Fetuses with 7q11.23 Microdeletion or Microduplication.
Dang Y; Wan S; Zheng Y; Song T; Li C; Li Y; Zhang J
Fetal Pediatr Pathol; 2020 Aug; 39(4):269-276. PubMed ID: 31402733
[No Abstract] [Full Text] [Related]
13. [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]
14. 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]
15. 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]
16. Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family.
Tang W; Chen G; Xia J; Zhang Y
Mol Cytogenet; 2022 Jul; 15(1):28. PubMed ID: 35787815
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Pathogenic recurrent copy number variants in 7,078 pregnancies via chromosomal microarray analysis.
Kang H; Chen Y; Wang L; Gao C; Li X; Hu Y
J Perinat Med; 2024 Feb; 52(2):171-180. PubMed ID: 38081620
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
Huang R; Fu F; Zhou H; Zhang L; Lei T; Cheng K; Yan S; Guo F; Wang Y; Ma C; Li R; Yu Q; Deng Q; Li L; Yang X; Han J; Li D; Liao C
Hum Genet; 2023 Jun; 142(6):835-847. PubMed ID: 37095353
[TBL] [Abstract][Full Text] [Related]
20. Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study.
Guo N; Xue H; Liang B; Huang H; Cai M; Xu L
BMC Med Genomics; 2023 Aug; 16(1):197. PubMed ID: 37612587
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
