Phenotype profiling of patients with intellectual disability and copy number variations
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
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3. Genetic diagnostic approach to intellectual disability and multiple congenital anomalies in Indonesia;Intractable & Rare Diseases Research;2023-05-31
4. Utility of whole‐exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population;Molecular Genetics & Genomic Medicine;2023-02-27
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
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