Charting the Path: Navigating Embryonic Development to Potentially Safeguard against Congenital Heart Defects
Journal of Personalized Medicine
journal-article
Charting the Path: Navigating Embryonic Development to Potentially Safeguard against Congenital Heart Defects
Journal of Personalized Medicine
journal-article
Charting the Path: Navigating Embryonic Development to Potentially Safeguard against Congenital Heart Defects
Journal of Personalized Medicine
journal-article
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome
Genes
journal-article
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome
Genes
journal-article
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome
Genes
journal-article
Internship Report at the Giannina Gaslini Institute
Istituto Giannina Gaslini
dissertation-thesis
NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint
Life
journal-article
NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint
Life
journal-article
NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint
Life
journal-article