Ala|Mello S

Institution: , N/A

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

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