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A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration

Predicted Benign and Synonymous variants in CYP11A1 Causes Primary Adrenal Insufficiency through Missplicing

Copy number variation: a prognostic marker for young patients with squamous cell carcinoma of the oral tongue

Copy number variation: a prognostic marker for young patients with squamous cell carcinoma of the oral tongue

Detecting Genetics Modifiers of Spondyloepimetaphyseal Dysplasia with Joint Laxity (SEMDJL) in the Caucasian Afrikaner community

Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type Maroteaux

The gut microbiome of Mexican children affected by obesity

Human serum albumin alters specific genes that can play a role in survival and persistence in Acinetobacter baumannii

Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature

A splice site variant in INPP5E causes diffuse cystic renal dysplasia and hepatic fibrosis in dogs

Organism-environment interactions and differential gene expression patterns among open-coastal and estuarine populations of Porphyra umbilicalis Kützing (Rhodophyta) in the Northwest Atlantic

Distinct clinical and pathological features of melorheostosis associated with somatic MAP2K1 mutations

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