Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies-Reference-Cited by-同舟云学术

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Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies

Published:2014-12 Issue:4 Volume:53 Page:579-582
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Li Ru,Fu Fang,Zhang Yong-Ling,Li Dong-Zhi,Liao Can

Funder

National Natural Science Foundation of China

Guangzhou Science and Technology Bureau Project

Guangdong Provincial Medical Research Foundation

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference22 articles.

1. Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys;Decramer;J Am Soc Nephrol,2007

2. Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy;Mefford;Am J Hum Genet,2007

3. Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12;Nagamani;Eur J Hum Genet,2010

4. 17q12 microdeletion syndrome: three patients illustrating the phenotypic spectrum;Dixit;Am J Med Genet A,2012

5. Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion;Loirat;Nephrol Dial Transplant,2010

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Fetal MRI Analysis of Corpus Callosal Abnormalities: Classification, and Associated Anomalies;Diagnostics;2024-02-15

2. 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

3. Tekrarlayan Düşüklerde Array Karşılaştırmalı Genomic Hibridizasyonun Yapısal Anomalileri Saptamadaki Önemi: Retrospektif Bir Çalışma;Adnan Menderes Üniversitesi Sağlık Bilimleri Fakültesi Dergisi;2023-09-30

4. Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing;Human Genetics;2023-04-24

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

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