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UnknownThe Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3).
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S-EPMC9778410 | biostudies-literature
UnknownA novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations.
Not available
S-EPMC6732295 | biostudies-literature
UnknownDeleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations.
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S-EPMC6862269 | biostudies-literature
UnknownMutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
Not available
S-EPMC3882911 | biostudies-literature
UnknownVariants in KIAA0825 underlie autosomal recessive postaxial polydactyly.
Not available
S-EPMC6724712 | biostudies-literature
UnknownAdaptive Randomization of Neratinib in Early Breast Cancer.
Not available
S-EPMC5259558 | biostudies-literature
UnknownAdaptive Randomization of Veliparib-Carboplatin Treatment in Breast Cancer.
Not available
S-EPMC5259561 | biostudies-literature
UnknownA benchmark of expert-level academic questions to assess AI capabilities.
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S-EPMC12851929 | biostudies-literature
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