Author:
Sankhyan Naveen,Kasinathan Ananthanarayanan,Dijk TessaVan,Singh Paramjeet,Singhi Pratibha
Subject
General Neuroscience,Pediatrics, Perinatology, and Child Health
Cited by
7 articles.
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1. Case report: A severe clinical phenotype of pontocerebellar hypoplasia type 7 with compound heterozygous variants of TOE1;Heliyon;2024-04
2. Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonology;Italian Journal of Pediatrics;2023-09-08
3. Genetic and prenatal diagnosis of a Chinese pedigree with pathogenic
TOE1
variants causing pontocerebellar hypoplasia type 7;The Journal of Maternal-Fetal & Neonatal Medicine;2023-08-27
4. Novel compound heterozygous missense variants in TOE1 gene associated with pontocerebellar hypoplasia type 7;Gene;2023-04
5. Delineating the phenotype and genetic basis of AMPD2-related pontocerebellar hypoplasia;neurogenetics;2022-11-29