Werner syndrome
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- Epigenetic Signatures of Werner Syndrome Occur Early in Life and Are Distinct from Normal Epigenetic Aging Processes
- Early Onset Werner Syndrome
- Inherigen Plus Carrier Screen Disease List
- Altered Nuclear Functions in Progeroid Syndromes: a Paradigm for Aging Research
- Carrier Detection of Werner's Syndrome Using a Microsatellite That Exhibits Linkage Disequilibrium with the Werner's Syndrome Locus
- Exome Sequencing Reveals a De Novo POLD1 Mutation Causing Phenotypic Variability in Mandibular Hypoplasia, Deafness, Progeroid F
- Mismatch Repair in Extracts of Werner Syndrome Cell Lines
- Hereditary Nonmelanoma Skin Cancer Vasiliki Nikolaou, MD,* Alexander J
- The Werner Syndrome Protein Has Separable Recombination and Survival Functionsଝ
- Mismatch Repair in Extracts of Werner Syndrome Cell Lines
- WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
- Adermatoglyphia: Challenges and Prospects in Diagnosis
- Review Werner's Syndrome: from Clinics to Genetics
- Insights from Progeroid Syndromes Into Skin Cancer and Aging Brian C
- Hallmarks of Progeroid Syndromes: Lessons from Mice and Reprogrammed Cells Dido Carrero, Clara Soria-Valles and Carlos López-Otıń*
- WES Gene Package Multiple Congenital Anomalie
- Bloom's Syndrome and the Ataxia-Telangiectasia- Mutated Protein, ATM
- DNA Helicases and Human Disease