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2025
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2024
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2023
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2018
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Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders.
Not available
S-EPMC12633141
|
biostudies-literature
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Characterizing Long COVID in Children and Adolescents.
Not available
S-EPMC11339705
|
biostudies-literature
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Characterizing Long COVID Symptoms During Early Childhood.
Not available
S-EPMC12117493
|
biostudies-literature
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Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
Not available
S-EPMC7614484
|
biostudies-literature
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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Not available
S-EPMC6218476
|
biostudies-literature
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