Severe autosomal recessive disorder werner syndrome. Medical search. Frequent questions

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Anatomy8

Fibroblasts Telomere Chromosomes, Human, Pair 8 HeLa Cells Cell Line Chromosomes, Human, Pair 1 Cells, Cultured Chromosomes, Human, Pair 2

Diseases63

Werner Syndrome Syndrome Bloom Syndrome Abnormalities, Multiple Rothmund-Thomson Syndrome Aging, Premature Albinism, Oculocutaneous Progeria Cystinosis Hermanski-Pudlak Syndrome Lipoid Proteinosis of Urbach and Wiethe Microcephaly Bardet-Biedl Syndrome Intellectual Disability Dwarfism Osteochondrodysplasias Metabolism, Inborn Errors Polycystic Kidney, Autosomal Recessive Papillon-Lefevre Disease Amino Acid Metabolism, Inborn Errors Retinitis Pigmentosa Hearing Loss, Sensorineural Hypotrichosis Usher Syndromes Fanconi Anemia Ataxia Telangiectasia Chediak-Higashi Syndrome Muscular Atrophy, Spinal Afibrinogenemia Hepatolenticular Degeneration Urea Cycle Disorders, Inborn Nails, Malformed Ichthyosis, Lamellar Facies Ellis-Van Creveld Syndrome Spinal Muscular Atrophies of Childhood Porphyria, Erythropoietic Lipid Metabolism, Inborn Errors Anemia, Megaloblastic Hypopigmentation Craniofacial Abnormalities Genetic Diseases, Inborn Hair Diseases Lipodystrophy, Congenital Generalized Muscular Dystrophies Deafness Wolfram Syndrome Hemochromatosis Alkaptonuria Genomic Instability Mitochondrial Encephalomyopathies Chromosome Disorders Malabsorption Syndromes Down Syndrome Metabolic Syndrome X Acrodermatitis Polydactyly Rare Diseases Pseudoxanthoma Elasticum Adrenal Hyperplasia, Congenital Ichthyosis Growth Disorders Lacrimal Apparatus Diseases

Chemicals and Drugs26

RecQ Helicases Exodeoxyribonucleases DNA Helicases Exonucleases 4-Nitroquinoline-1-oxide DNA Adenosine Triphosphatases Codon, Nonsense Survival of Motor Neuron 1 Protein DNA-Binding Proteins Replication Protein A Telomeric Repeat Binding Protein 2 Genetic Markers SMN Complex Proteins Proton-Coupled Folate Transporter Antigens, Nuclear Membrane Proteins Cathepsin C Nuclear Proteins Solute Carrier Family 12, Member 3 Proteins Recombinant Proteins Uroporphyrinogen III Synthetase DNA, Single-Stranded Carbon-Carbon Ligases Ceruloplasmin

Analytical, Diagnostic and Therapeutic Techniques and Equipment11

Pedigree DNA Mutational Analysis Chromosome Mapping Heterozygote Detection Genetic Testing Facies Polymerase Chain Reaction Models, Genetic Fatal Outcome Prenatal Diagnosis Sequence Analysis, DNA

Psychiatry and Psychology5

Intellectual Disability Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders

Phenomena and Processes39

Genes, Recessive Consanguinity Mutation Homozygote Phenotype Mutation, Missense Heterozygote Base Sequence Genetic Linkage DNA Damage Lod Score Exons Telomere Codon, Nonsense Frameshift Mutation DNA Replication DNA Repair Amino Acid Sequence Haplotypes Founder Effect Chromosomes, Human, Pair 8 Genetic Heterogeneity Alleles Genotype Polymorphism, Single-Stranded Conformational Genetic Markers Protein Structure, Tertiary Point Mutation Protein Binding Chromosomes, Human, Pair 1 Microsatellite Repeats Recombination, Genetic Chromosomes, Human, Pair 2 Genomic Instability Sequence Deletion Cell Aging DNA, Single-Stranded Genes, Dominant Aging

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Fatal Outcome

Named Groups2

Infant, Newborn Jews

Health Care3

Genetic Testing Family Health Fatal Outcome

Geographicals2

Pakistan Lebanon

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care Geographicals

Werner Syndrome RecQ Helicases Genes, Recessive Exodeoxyribonucleases Syndrome DNA Helicases Consanguinity Pedigree Mutation Bloom Syndrome Homozygote Abnormalities, Multiple Exonucleases DNA Mutational Analysis Rothmund-Thomson Syndrome Aging, Premature Phenotype 4-Nitroquinoline-1-oxide Albinism, Oculocutaneous Mutation, Missense Molecular Sequence Data Progeria DNA Heterozygote Base Sequence Cystinosis Hermanski-Pudlak Syndrome Chromosome Mapping Genetic Linkage Lipoid Proteinosis of Urbach and Wiethe Microcephaly Adenosine Triphosphatases DNA Damage Lod Score Bardet-Biedl Syndrome Exons Intellectual Disability Dwarfism Fibroblasts Telomere Heterozygote Detection Osteochondrodysplasias Metabolism, Inborn Errors Codon, Nonsense Frameshift Mutation DNA Replication DNA Repair Polycystic Kidney, Autosomal Recessive Amino Acid Sequence Papillon-Lefevre Disease Haplotypes Amino Acid Metabolism, Inborn Errors Founder Effect Survival of Motor Neuron 1 Protein Chromosomes, Human, Pair 8 Retinitis Pigmentosa Hearing Loss, Sensorineural Genetic Heterogeneity Alleles Hypotrichosis Usher Syndromes DNA-Binding Proteins Genotype Fanconi Anemia Ataxia Telangiectasia Chediak-Higashi Syndrome Genetic Testing Replication Protein A Telomeric Repeat Binding Protein 2 HeLa Cells Muscular Atrophy, Spinal Afibrinogenemia Hepatolenticular Degeneration Urea Cycle Disorders, Inborn Nails, Malformed Polymorphism, Single-Stranded Conformational Genetic Markers Ichthyosis, Lamellar Family Health Cell Line Facies Ellis-Van Creveld Syndrome Infant, Newborn Spinal Muscular Atrophies of Childhood Porphyria, Erythropoietic Protein Structure, Tertiary Lipid Metabolism, Inborn Errors Point Mutation Protein Binding Anemia, Megaloblastic Hypopigmentation Bipolar Disorder SMN Complex Proteins Craniofacial Abnormalities Proton-Coupled Folate Transporter Chromosomes, Human, Pair 1 Genetic Diseases, Inborn Hair Diseases Microsatellite Repeats Lipodystrophy, Congenital Generalized

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