A recognizable phenotype related to 19p13.12 microdeletion-Reference-Cited by-同舟云学术

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A recognizable phenotype related to 19p13.12 microdeletion

Published:2018-07-28 Issue:8 Volume:176 Page:1753-1759
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet Part A

Author:

de Souza Laiara Cristina¹,Sgardioli Ilária Cristina¹,Gil-da-Silva-Lopes Vera Lúcia¹^ORCID,Vieira Társis Paiva¹^ORCID

Affiliation:

1. Department of Medical Genetics, Faculty of Medical Sciences; State University of Campinas (UNICAMP); Campinas Brazil

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38842/fullpdf

Reference28 articles.

1. Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions;Bonaglia;European Journal of Human Genetics,2010

2. Targeting protein-protein interactions in complexes organized by A kinase anchoring proteins;Calejo;Frontiers in Pharmacology,2015

3. Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: A single-centre study;Dale;Developmental Medicine & Child Neurology,2012

4. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects;Donato;BMC Medicine,2017

5. Protein kinase A-anchoring protein AKAP95 interacts with MCM2, a regulator of DNA replication;Eide;Journal of Biological Chemistry,2003

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