Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome.
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| Title: | Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome. |
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| Authors: | Maharaj AV; Centre for Endocrinology, William Harvey Research Institute, QMUL, London, United Kingdom., Cottrell E; Centre for Endocrinology, William Harvey Research Institute, QMUL, London, United Kingdom., Thanasupawat T; Department of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, Manitoba, Canada., Joustra SD; Division of Paediatric Endocrinology, Department of Paediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Centre, Leiden, Netherlands., Triggs-Raine B; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada., Fujimoto M; Cincinnati Center for Growth Disorders, Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, USA., Kant SG; Division of Paediatric Endocrinology, Department of Paediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Centre, Leiden, Netherlands., van der Kaay D; Division of Paediatric Endocrinology, Department of Paediatrics, Erasmus University Medical Centre, Sophia Children's Hospital, Rotterdam, Netherlands., Clement-de Boers A; Department of Paediatrics, Juliana Children's Hospital/Haga Teaching Hospital, The Hague, Netherlands., Brooks AS; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, Netherlands., Aguirre GA; CITES - Escuela Nacional de Medicina, TEC de Monterrey, Monterrey, Nuevo León, Mexico., Martín Del Estal I; CITES - Escuela Nacional de Medicina, TEC de Monterrey, Monterrey, Nuevo León, Mexico., Castilla de Cortázar Larrea MI; CITES - Escuela Nacional de Medicina, TEC de Monterrey, Monterrey, Nuevo León, Mexico., Massoud A; Department of Paediatrics and Child Health, HCA Healthcare UK, London, United Kingdom., van Duyvenvoorde HA; Laboratory for Diagnostic Genome analysis (LDGA), Department of Clinical Genetics, Leiden University Medical Centre, Leiden, Netherlands., De Bruin C; Division of Paediatric Endocrinology, Department of Paediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Centre, Leiden, Netherlands., Hwa V; Cincinnati Center for Growth Disorders, Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, USA., Klonisch T; Department of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, Manitoba, Canada.; Department of Pathology, and.; Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada., Hombach-Klonisch S; Department of Human Anatomy and Cell Science, University of Manitoba, Winnipeg, Manitoba, Canada.; Department of Pathology, and., Storr HL; Centre for Endocrinology, William Harvey Research Institute, QMUL, London, United Kingdom. |
| Source: | JCI insight [JCI Insight] 2024 Feb 20; Vol. 9 (6). Date of Electronic Publication: 2024 Feb 20. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 101676073 Publication Model: Electronic Cited Medium: Internet ISSN: 2379-3708 (Electronic) Linking ISSN: 23793708 NLM ISO Abbreviation: JCI Insight Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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