YEAR 2024 VOLUME 2 ISSUE 3
Published:
2024-12-05
Hypotonic syndrome as a manifestation of an ultra-rare disease caused by a new and de novo variant in the PLA2G6 gene
De novo variant in the COL1A1 gene associated with orphan genetic disease: Osteogenesis Imperfecta type I
De novo genetic variant in epileptic encephalopathy: Importance of specific diagnosis
Detection of a genetic variant of Apert syndrome
Advances and Perspectives of Genetic Pathologies in the 21st century.
eISSN L 3072-9610 (English)
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