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Medicine & Life Sciences

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

Chemical Compounds

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