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
 
		
							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 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
 
		
							De novo genetic variant in epileptic encephalopathy: Importance of specific diagnosis
																			
		
	 Detection of a genetic variant of Apert syndrome
 
		
							Detection of a genetic variant of Apert syndrome
																			
		
	 Advances and Perspectives of Genetic Pathologies in the 21st century.
 
		
							Advances and Perspectives of Genetic Pathologies in the 21st century.
																			
		
	eISSN L 3072-9610 (English)
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