Ala|Mello S

Institution: , N/A

Top Collaborators: Ala-mello S, Torniainen S, Devriendt K, Fryns JP, Marynen P, Järvelä I, Castrén M, Gaily E, Tengström C, Lähdetie J, Froyen G, Archer H, Govaerts K, Van Esch H, Verbeeck J, Tuomi ML, Heikkilä H

Research Interests: Gene, Mutation, Mutations, Patients, Phenotypes, Acids, Amino Acids, Chromosomes, Coding, Exon, Eyes, Focal Dermal Hypoplasia, Genes, Goltz-gorlin Syndrome, Gorlin Syndrome, Limb, Literature, Missense Mutations, PCR, Point Mutations