A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation—Case Report With Literature Review-Reference-Cited by-同舟云学术

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A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation—Case Report With Literature Review

Published:2019-07-08 Issue: Volume:7 Page:
ISSN:2296-2360
Container-title:Frontiers in Pediatrics
language:
Short-container-title:Front. Pediatr.

Author:

Chirita Emandi Adela,Dobrescu Andreea Iulia,Doros Gabriela,Hyon Capucine,Miclea Diana,Popoiu Calin,Puiu Maria,Arghirescu Smaranda

Funder

Autoritatea Natională pentru Cercetare Stiintifică

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations;Rossi;J Med Genet.,2001

2. Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review;Quintero-Rivera;Am J Med Genet A.,2010

3. 3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome;Willatt;Am J Hum Genet.,2005

4. Copy number variation in bipolar disorder;Green;Mol Psychiatry,2016

5. Novel features of 3q29 deletion syndrome: results from the 3q29 registry;Glassford;Am J Med Genet A,2016

Cited by 8 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. Intrapericardial Teratoma and Associated 3q29 Deletion in a Fetus: Case Report;Zeitschrift für Geburtshilfe und Neonatologie;2024-08-20

2. A critical review of the impact of candidate copy number variants on autism spectrum disorder;Mutation Research - Reviews in Mutation Research;2024-07

3. Phenotypes for general behavior, activity, and body temperature in 3q29 deletion model mice;Translational Psychiatry;2024-03-07

4. Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return;European Journal of Human Genetics;2023-09-07

5. Structural deviations of the posterior fossa and the cerebellum and their cognitive links in a neurodevelopmental deletion syndrome;2022-03-02

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