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Medicine & Life Sciences

Mutation
Pantothenate Kinase-Associated Neurodegeneration
Genes
Neoplasms
Fanconi Anemia
DNA Mismatch Repair
Phenylketonurias
Genome
Proteins
Microfibrils
Phenotype
Copper
DNA
Breast Neoplasms
Anhidrotic Ectodermal Dysplasia 1
Inborn Urea Cycle Disorder
Therapeutics
Genetic Testing
Marfan Syndrome
Iron
Chromosomes
Exome
Brain
Phenylalanine
Ectodermal Dysplasia
Fibroblasts
Atlases
Protein Phosphatase 2
Missense Mutation
Cell Line
Medical Genetics
Inborn Genetic Diseases
Neurodegenerative Diseases
Liver
Alleles
Research
Phenylalanine Hydroxylase
Fatty Acids
Genomics
DNA Damage
Skin
Genetic Therapy
Cytogenetics
Neuroaxonal Dystrophies
Growth
Hepatocytes
Connective Tissue
Transforming Growth Factors
Proto-Oncogene Proteins c-myc
Yeasts
Coenzyme A
Fluorescence In Situ Hybridization
Exons
Ubiquitination
Genomic Instability
Dystonia
Phosphorylation
Globus Pallidus
Chromatin
DNA Repair
Carcinogenesis
Pregnancy
Ubiquitin
Aneuploidy
Gene Expression
Apoptosis
Saccharomyces cerevisiae
Chromosome Aberrations
Genetic Recombination
Cell Cycle
Inborn Errors Metabolism
Molecular Biology
Enzymes
Autistic Disorder
Extracellular Matrix
Guidelines
Mutation Rate
Elastin
Oncogene Proteins
Fanconi Anemia Complementation Group Proteins
Newborn Infant
Colorectal Neoplasms
Meiosis
Mothers
Tumor Suppressor Proteins
Parkinsonian Disorders
Adenocarcinoma
Carnitine O-Palmitoyltransferase
Population
Carrier Proteins
Glioblastoma
Metals
Mitomycin
Messenger RNA
Cell Proliferation
3-Hydroxyacyl-CoA Dehydrogenase
DNA Mutational Analysis
Intercellular Signaling Peptides and Proteins
Diet
Hepatolenticular Degeneration

Chemical Compounds

Genes
Tumors
Cells
Copper
Repair
Proteins
DNA
Tissue
Chemical activation
Yeast
Brain
Phenylalanine
Blood
Nutrition
Phosphorylation
Ubiquitin
Liver
Degradation
Urea
Transcription
Assays
Azurin
Chromosomes
Apoptosis
Ribosomal Proteins
Metabolism
Fibroblasts
Enzymes
Metals
Carrier Proteins
3-Hydroxyacyl-CoA Dehydrogenase