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Medicine & Life Sciences

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

Chemical Compounds

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