Recurrent microdeletion 2q21.1: Report on a new patient with neurological disorders-Reference-Cited by-同舟云学术

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Recurrent microdeletion 2q21.1: Report on a new patient with neurological disorders

Published:2013-12-20 Issue:3 Volume:164 Page:801-805
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gimelli Stefania¹,Stathaki Elisavet¹,Béna Frédérique¹,Leoni Massimiliano²,Di Rocco Maja³,Cuoco Cristina⁴,Tassano Elisa⁴

Affiliation:

1. Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland

2. Pediatria II; Istituto G Gaslini; Genova Italy

3. USD Malattie Rare; Istituto G Gaslini; Genova Italy

4. Laboratorio di Citogenetica; Istituto Giannina Gaslini; Genova Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. Diffuse malformations of cortical development;Bahi-Buisson;Handb Clin Neurol,2013

2. Expression patterns of the Wtx/Amer gene family during mouse embryonic development;Comai;Dev Dyn,2010

3. Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148;Dharmadhikari;Hum Mol Genet,2012

4. The evolutionarily conserved G protein-coupled receptor SREB2/GPR85 influences brain size, behavior, and vulnerability to schizophrenia;Matsumoto;Proc Natl Acad Sci USA,2008

5. Effect of Schizophrenia risk-associated alleles in SREB2 (GPR85) on functional MRI phenotypes in healthy volunteers;Radulescu;Neuropsychopharmacology,2013

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1. Prenatal Diagnosis of a de novo 2q14.3-q22.1 Deletion with Complex Chromosomal Rearrangement;Molecular Syndromology;2023-09-18

2. Structural variation in families with speech and language disorder provides a deeper understanding of the genetic basis for naturally acquired speech;2023-05-31

3. Genome-wide screening for genetic variants in polyadenylation signal (PAS) sites in mouse selection lines for fatness and leanness;Mammalian Genome;2022-11-21

4. A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review;Molecular Genetics & Genomic Medicine;2020-01-28

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