Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability-Reference-Cited by-同舟云学术

Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability

Published:2017-06 Issue: Volume:185 Page:160-166.e1
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Heide Solveig^ORCID,Keren Boris,Billette de Villemeur Thierry,Chantot-Bastaraud Sandra,Depienne Christel,Nava Caroline,Mignot Cyril,Jacquette Aurélia,Fonteneau Eric,Lejeune Elodie,Mach Corinne,Marey Isabelle,Whalen Sandra,Lacombe Didier,Naudion Sophie,Rooryck Caroline,Toutain Annick,Caignec Cédric Le,Haye Damien,Olivier-Faivre Laurence,Masurel-Paulet Alice,Thauvin-Robinet Christel,Lesne Fabien,Faudet Anne,Ville Dorothée,des Portes Vincent,Sanlaville Damien,Siffroi Jean-Pierre,Moutard Marie-Laure,Héron Delphine

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference34 articles.

1. Variability of homotopic and heterotopic callosal connectivity in partial agenesis of the corpus callosum: a 3T diffusion tensor imaging and Q-ball tractography study;Wahl;AJNR Am J Neuroradiol,2009

2. Major brain lesions detected on sonographic screening of apparently normal term neonates;Wang;Neuroradiology,2004

3. Evaluation of the child with idiopathic mental retardation;Schaefer;Pediatr Clin North Am,1992

4. Children with agenesis of the corpus callosum;Grogono;Dev Med Child Neurol,1968

5. Agenesis of the corpus callosum: a clinical approach to diagnosis;Palmer;Am J Med Genet C Semin Med Genet,2014

Cited by 26 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. Prenatal Diagnosed Agenesis of the Corpus Callosum: Identifying the Underlying Genetic Etiologies;Prenatal Diagnosis;2024-08-08

2. Fetal agenesis of the corpus callosum: Clinical and genetic analysis in a series of 40 patients;European Journal of Obstetrics & Gynecology and Reproductive Biology;2024-07

3. Loss-of-function variants inZEB1cause dominant anomalies of the corpus callosum with favourable cognitive prognosis;Journal of Medical Genetics;2023-10-19

4. Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature;Genes;2023-01-02

5. Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort;Diagnostics;2022-12-12