A ZFHX4 mutation associated with a recognizable neuropsychological and facial phenotype-Reference-Cited by-同舟云学术

A ZFHX4 mutation associated with a recognizable neuropsychological and facial phenotype

Published:2021-11 Issue:11 Volume:64 Page:104321
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Fontana Paolo^ORCID,Ginevrino Monia^ORCID,Bejo Kristel^ORCID,Cantalupo Giuseppina,Ciavarella Maria,Lombardi Cinzia,Maioli Marianna,Scarano Francesca,Costabile Claudia^ORCID,Novelli Antonio^ORCID,Lonardo Fortunato^ORCID

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference18 articles.

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2. Familial occurrence of ptosis, nasal speech, prominent ears, hand anomalies and learning problems;Belligni;Eur. J. Med. Genet.,2010

3. ZFHX4 interacts with the NuRD core member CHD4 and regulates the glioblastoma tumor initiating cell state;Chudnovsky;Cell Rep.,2014

4. A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development;Eising;Mol. Psychiatr.,2019

5. 8q21.11 microdeletion in two patients with syndromic peters anomaly;Happ;Am. J. Med. Genet.,2016

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1. Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder;2024-08-08

2. Genetic architecture of childhood speech disorder: a review;Molecular Psychiatry;2024-02-16

3. Ocular Manifestations of Peters Plus-Like Syndrome in 8q21.11 Microdeletion Syndrome;Cornea;2023-04-06

4. Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10;American Journal of Medical Genetics Part A;2023-01-03

5. Congenital corneal staphyloma in 8q21.11 microdeletion syndrome;Ophthalmic Genetics;2022-11-07