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Por um escritor misterioso
Last updated 30 julho 2024
Neurologic, Neuropsychologic, and Neuroradiologic Features of EBF3-Related Syndrome
Genetic Leukoencephalopathies in Adults. - Abstract - Europe PMC
A CUreaOus Case of Post-Partum Hepatic Encephalopathy - SHM Abstracts
Mcleod Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
PDF) The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)
Advanced genomics v_medical_pitt_kent_osu
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14 - ScienceDirect
Genetics and Prader-Willi Syndrome — Know Rare
MedGen - NCBI Resources - Library Guides at UChicago
DDC Clinic ~ Center for Special Needs Children
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