Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.
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| Title: | Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders. |
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| Authors: | Wootton O; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Campbell P; Department of Medical and Molecular Genetics, King's College London, London, UK., Richardson S; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK., Lindsay SJ; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Huang QQ; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Delage E; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Amanat S; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Wong HS; Cambridge University Hospitals Foundation Trust, Addenbrooke's Hospital, Cambridge, UK., Firth HV; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.; Cambridge University Hospitals Foundation Trust, Addenbrooke's Hospital, Cambridge, UK., Hurles ME; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Simpson MA; Department of Medical and Molecular Genetics, King's College London, London, UK., Radford EJ; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.; Department of Paediatrics, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK., Martin HC; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK. hcm@sanger.ac.uk. |
| Source: | Genome medicine [Genome Med] 2025 Oct 30; Vol. 17 (1), pp. 134. Date of Electronic Publication: 2025 Oct 30. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1756-994X |
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| DOI: | 10.1186/s13073-025-01560-3 |
