Insertional translocation leading to a 4q13 duplication including theEPHA5gene in two siblings with attention-deficit hyperactivity disorder-Reference-Cited by-同舟云学术

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Insertional translocation leading to a 4q13 duplication including theEPHA5gene in two siblings with attention-deficit hyperactivity disorder

Published:2013-07-04 Issue:8 Volume:161 Page:1923-1928
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Matoso Eunice,Melo Joana B.,Ferreira Susana I.¹,Jardim Ana¹,Castelo Teresa M.²,Weise Anja³,Carreira Isabel M.

Affiliation:

1. Laboratory of Cytogenetics and Genomics, Faculty of Medicine; University of Coimbra; Coimbra; Portugal

2. Child Development Center; Paediatrics Hospital; Coimbra; Portugal

3. Jena University Hospital; Institute of Human Genetics; Kollegiengasse; Jena; Germany

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36032/fullpdf

Reference24 articles.

1. Molecular genetics of attention-deficit/hyperactivity disorder: An overview;Banaschewski;Eur Child Adolesc Psychiatry,2010

2. A synaptic model of memory: Longterm potentiation in the hippocampus;Bliss;Nature,1993

3. Characterization of mosaic supernumerary ring chromosomes by array-CGH: Segmental aneusomy for proximal 4q in a child with tall stature and obesity;Bonnet;Am J Med Genet Part A,2006

4. Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31→qter) detected in an autistic boy;Carreira;Mol Cytogenet,2009

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1. The Identification of Key Genes and Biological Pathways in Polycystic Ovary Syndrome and its Complications by Next Generation Squancing (NGS) and Bioinformatics Analysis;2023-01-02

2. A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature;Genes;2021-12-07

3. Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report;International Journal of Reproductive BioMedicine (IJRM);2021-06-23

4. Deep learning model reveals potential risk genes for ADHD, especially Ephrin receptor gene EPHA5;Briefings in Bioinformatics;2021-06-09

5. Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene;Psychiatric Genetics;2019-06

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