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-Reference-Cited by-同舟云学术

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

Published:2013-12 Issue:4 Volume:52 Page:551-557
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Chang Shuenn-Dyh,Wang Tzu-Hao,Wang Liang-Kai,Tsai Jeng-Daw,Liu Yu-Peng,Chern Schu-Rern,Wu Peih-Shan,Su Jun-Wei,Chen Yu-Ting,Wang Wayseen

Funder

National Science Council

Mackay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference50 articles.

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3. A molecular and genetic view of human renal and urinary tract malformations;Woolf;Kidney Int,2000

4. HNF1B alterations associated with congenital anomalies of the kidney and urinary tract;Nakayama;Pediatr Nephrol,2010

5. Copy-number disorders are a common cause of congenital kidney malformations;Sanna-Cherchi;Am J Hum Genet,2012

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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. Clinico-morphological phenotype and genotype of multicystic kidney dysplasia in children;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2024-05-08

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. Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions;Prenatal Diagnosis;2023-08-26

5. Potter Deformation Sequence Caused by 17q12 Deletion: A Lethal Constellation;Pediatric and Developmental Pathology;2022-12-13