Clinical and molecular findings of the six patients with Rubinstein
Por um escritor misterioso
Last updated 11 abril 2025


An investigational oral plasma kallikrein inhibitor for on-demand treatment of hereditary angioedema: a two-part, randomised, double-blind, placebo-controlled, crossover phase 2 trial - The Lancet

Novel suprasellar location of desmoplastic infantile astrocytoma and ganglioglioma: a single institution's experience in: Journal of Neurosurgery: Pediatrics Volume 22 Issue 4 (2018) Journals

Molecular insights may inform new treatments for drug-resistant tuberculosis

Genetic basis of mitochondrial diseases - Gusic - 2021 - FEBS Letters - Wiley Online Library

Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Genes, Free Full-Text

Images showing classical RSTS features of patient including thickened

IJMS, Free Full-Text

Computational and Structural Analysis to Assess the Pathogenicity of Bardet-Biedl Syndrome Related Missense Variants Identified in Bardet-Biedl Syndrome 10 Gene (BBS10)
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