Ala|Mello S

Institution: , N/A

Top Collaborators: Ala-mello S, Tuomi ML, Heikkilä H, 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

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