Copy number variations in multicystic dysplastic kidney: update for prenatal diagnosis and genetic counseling-Reference-Cited by-同舟云学术

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Copy number variations in multicystic dysplastic kidney: update for prenatal diagnosis and genetic counseling

Published:2016-04-02 Issue:5 Volume:36 Page:463-468
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Xi Qi¹,Zhu Xiangyu¹,Wang Yaping²,Ru Tong¹,Dai Chenyan¹,Wang Zhiqun¹,Li Jie³,Hu Yali¹

Affiliation:

1. Department of Obstetrics and Gynecology; Drum Tower Hospital, Medical School of Nanjing University; Nanjing Jiangsu China

2. Department of Medical Genetics, Jiangsu Key Laboratory of Molecular Medicine, Medical School of Nanjing University; Nanjing Jiangsu China

3. Centre of Prenatal Diagnosis of Jiangsu Province, Drum Tower Hospital; Medical School of Nanjing University; Nanjing Jiangsu China

Funder

Science and Technology Department of Jiangsu Province

Key Laboratory for Maternal-Fetal Medicine from the Health Department of Jiangsu Province, China

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4807/fullpdf

Reference27 articles.

1. Dysplastic kidneys;Winyard;Semin Fetal Neonatal Med,2008

2. Unilateral multicystic dysplastic kidney: a meta-analysis of observational studies on the incidence, associated urinary tract malformations and the contralateral kidney;Schreuder;Nephrol Dial Transplant,2009

3. Update on multicystic dysplastic kidney;Cardona-Grau;Curr Urol Rep,2015

4. Prenatal diagnosis of fetal multicystic dysplastic kidney in the era of three-dimensional ultrasound: 10-year experience;Hsu;Taiwan J Obstet Gynecol,2012

5. Prenatal diagnosis of multicystic dysplastic kidney disease in the second trimester screening;Al Naimi;Prenat Diagn,2013

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1. Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review;Heliyon;2024-09

2. Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype–phenotype correlations;American Journal of Obstetrics & Gynecology MFM;2024-01

3. 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;Taiwanese Journal of Obstetrics and Gynecology;2024-01

4. Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions;Journal of Perinatal Medicine;2023-10-18

5. Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis;BMC Medical Genomics;2023-05-30

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