![Host genetics role in the pathogenesis of periodontal disease and caries - Nibali - 2017 - Journal of Clinical Periodontology - Wiley Online Library Host genetics role in the pathogenesis of periodontal disease and caries - Nibali - 2017 - Journal of Clinical Periodontology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c677369a-8824-4175-a473-c1ccce17036e/jcpe12639-fig-0001-m.jpg)
Host genetics role in the pathogenesis of periodontal disease and caries - Nibali - 2017 - Journal of Clinical Periodontology - Wiley Online Library
![RNA exosome mutations in pontocerebellar hypoplasia alter ribosome biogenesis and p53 levels | Life Science Alliance RNA exosome mutations in pontocerebellar hypoplasia alter ribosome biogenesis and p53 levels | Life Science Alliance](https://www.life-science-alliance.org/sites/default/files/highwire/lsa/3/8.cover-source.jpg)
RNA exosome mutations in pontocerebellar hypoplasia alter ribosome biogenesis and p53 levels | Life Science Alliance
![GEnomes Management Application (GEM.app): A New Software Tool for Large‐Scale Collaborative Genome Analysis - Gonzalez - 2013 - Human Mutation - Wiley Online Library GEnomes Management Application (GEM.app): A New Software Tool for Large‐Scale Collaborative Genome Analysis - Gonzalez - 2013 - Human Mutation - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/2f0e6bae-ba72-4eea-9a07-3d3b3287ed96/humu22305-gra-0001-m.jpg)
GEnomes Management Application (GEM.app): A New Software Tool for Large‐Scale Collaborative Genome Analysis - Gonzalez - 2013 - Human Mutation - Wiley Online Library
![A MEISSEN BÖTTGER PORCELAIN TEABOWL AND SAUCER ATTRIBUTED TO IGNAZ PREISSLER - Rare CeramicsRare Ceramics A MEISSEN BÖTTGER PORCELAIN TEABOWL AND SAUCER ATTRIBUTED TO IGNAZ PREISSLER - Rare CeramicsRare Ceramics](https://www.rare-ceramics.com/wp-content/uploads/Preissler-iron-red-and-Swcwarzl-Tbowl-and-S-8-a.jpg)
A MEISSEN BÖTTGER PORCELAIN TEABOWL AND SAUCER ATTRIBUTED TO IGNAZ PREISSLER - Rare CeramicsRare Ceramics
![DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System - Sommen - 2016 - Human Mutation - Wiley Online Library DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System - Sommen - 2016 - Human Mutation - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/1a7a928a-dc95-4a13-b39f-7ab841cb04f0/humu22999-gra-0001-m.jpg)
DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System - Sommen - 2016 - Human Mutation - Wiley Online Library
![Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies - Dohrn - 2017 - Journal of Neurochemistry - Wiley Online Library Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies - Dohrn - 2017 - Journal of Neurochemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/6ec2a27d-d6f6-483c-b4a0-9e74a0235d3e/jnc14217-fig-0004-m.jpg)
Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies - Dohrn - 2017 - Journal of Neurochemistry - Wiley Online Library
![Inherited neuropathies with predominant upper limb involvement: genetic heterogeneity and overlapping pathologies.,European Journal of Neurology - X-MOL Inherited neuropathies with predominant upper limb involvement: genetic heterogeneity and overlapping pathologies.,European Journal of Neurology - X-MOL](https://xpic.x-mol.com/20200928%2F10.1111_ene.14514.jpg)
Inherited neuropathies with predominant upper limb involvement: genetic heterogeneity and overlapping pathologies.,European Journal of Neurology - X-MOL
![Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system. - Glia - X-MOL Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system. - Glia - X-MOL](https://xpic.x-mol.com/20200714%2F10.1002_glia.23805.jpg)
Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system. - Glia - X-MOL
![The role of tRNA synthetases in neurological and neuromuscular disorders - Boczonadi - 2018 - FEBS Letters - Wiley Online Library The role of tRNA synthetases in neurological and neuromuscular disorders - Boczonadi - 2018 - FEBS Letters - Wiley Online Library](https://febs.onlinelibrary.wiley.com/cms/asset/8d9e72f6-fbde-4ecc-a0ba-3b7edc26813c/feb212962-fig-0001-m.jpg)
The role of tRNA synthetases in neurological and neuromuscular disorders - Boczonadi - 2018 - FEBS Letters - Wiley Online Library
![Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing - Stals - 2018 - Prenatal Diagnosis - Wiley Online Library Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing - Stals - 2018 - Prenatal Diagnosis - Wiley Online Library](https://obgyn.onlinelibrary.wiley.com/cms/asset/57c36be6-96a4-42af-9572-311d9077c1da/pd5175-fig-0001-m.jpg)