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DMDD - Deciphering the Mechanisms of Developmental Disorders

Search free text comments. All ontologies/controlled vocabularies available. Exclude terms qualified as normal. Only suggest terms associated with current phenotype data. Go directly to page if only 1 result. The DMDD programme aims to study 'embryonic lethal' mouse mutations, and begin to understand why their mutation has such profound effects on embryo development and survival. Their study can also offer important insights into the origins of human developmental disorders. 201508 Release July 2015.

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DMDD - Deciphering the Mechanisms of Developmental Disorders | dmdd.org.uk Reviews
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Search free text comments. All ontologies/controlled vocabularies available. Exclude terms qualified as normal. Only suggest terms associated with current phenotype data. Go directly to page if only 1 result. The DMDD programme aims to study 'embryonic lethal' mouse mutations, and begin to understand why their mutation has such profound effects on embryo development and survival. Their study can also offer important insights into the origins of human developmental disorders. 201508 Release July 2015.
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DMDD - Deciphering the Mechanisms of Developmental Disorders | dmdd.org.uk Reviews

https://dmdd.org.uk

Search free text comments. All ontologies/controlled vocabularies available. Exclude terms qualified as normal. Only suggest terms associated with current phenotype data. Go directly to page if only 1 result. The DMDD programme aims to study 'embryonic lethal' mouse mutations, and begin to understand why their mutation has such profound effects on embryo development and survival. Their study can also offer important insights into the origins of human developmental disorders. 201508 Release July 2015.

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LATEST DATA RELEASE HIGHLIGHTS INCLUDING NEW HEART DEFECT ASSOCIATIONS. Oaz1 found to be associated with DORV, and Cc2d2a associated with VSD. Read more ». WHAT DOES NORMAL HEART DEVELOPMENT REALLY LOOK LIKE? A new publication considers the differences we might see between normal hearts as they grow. Read more ». 95 MILLION EMBRYO IMAGES NOW AVAILABLE. New embryonic lethal knockout mouse data released. Read more ». EDEMA – A SIGN OF UNDERLYING DEVELOPMENTAL DEFECTS. Read more ». Read more ».

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http://www.emouseatlas.org/emap

Analysis Tools & Resources. EMAGE Search & Analysis. Karl Theiler : The House Mouse. Cluster Data by Spatial Annotations. 3D rendering tool released for ts15-ts25. 3D models updated to v12 ontology (v13 for eHistology). Supplement with Coronal Sections. New 3D anatomy viewer using WebGL:. See the 9 day (Theiler 14) model. And click "3d view" at the top RHS. Release of Kaufman Supplement Atlas. Update of Kaufman Atlas terms to v12 ontology. 3D anatomy released for. Ts15, ts17, ts18 and ts19. 8226; EMA, th...

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eAtlas Links

http://www.emouseatlas.org/emap/eatlas_links/eatlas_links.html

Analysis Tools & Resources. EMAGE Search & Analysis. Karl Theiler : The House Mouse. Cluster Data by Spatial Annotations. Allen Institute for Brain Science. Of the Murine Head. The Mouse Brain Library. Atlas of Fetal Mouse. MR atlas of the. EMAP • Human Genetics Unit • Medical Research Council. Tel: 44(0)131 332 2471 • emap@emouseatlas.org. All site content, except where otherwise noted,. Is licensed under a Creative Commons Attribution License.

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DMDD - Deciphering the Mechanisms of Developmental Disorders

Search free text comments. All ontologies/controlled vocabularies available. Exclude terms qualified as normal. Only suggest terms associated with current phenotype data. Go directly to page if only 1 result. The DMDD programme aims to study 'embryonic lethal' mouse mutations, and begin to understand why their mutation has such profound effects on embryo development and survival. Their study can also offer important insights into the origins of human developmental disorders. 201508 Release July 2015.

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