Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil-Reference-Cited by-同舟云学术

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Molecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil

Published:2017 Issue:3 Volume:8 Page:155-160
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Nascimento Gustavo R.,Pinto Irene P.,de Melo Aldaires V.,da Cruz Damiana M.,Ribeiro Cristiano L.,da Silva Claudio C.,da Cruz Aparecido D.,Minasi Lysa B.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

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. The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases;Journal of Affective Disorders;2023-08

2. Genome-wide association study of cerebellar white matter microstructure and genetic overlap with common brain disorders;NeuroImage;2023-04

3. Role of androgen receptor signaling pathway-related lncRNAs in the prognosis and immune infiltration of breast cancer;Scientific Reports;2022-11-30

4. Koolen-de Vries syndrome: A de novo missense KANSL1 variant;Clinical Neurology and Neurosurgery;2022-11

5. Koolen‐de Vries syndrome in a 63‐year‐old woman: Report of the oldest patient and a review of the adult phenotype;American Journal of Medical Genetics Part A;2021-10-19

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