Associated Papers
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.
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Medrxiv : the Preprint Server for Health Sciences, 2025
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Supplement: media-1.xlsx › Supplementary_Table_3
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
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Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLMS08_het
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