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Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems

2011; Wiley; Volume: 155; Issue: 5 Linguagem: Inglês

10.1002/ajmg.a.33986

1552-4833

Adam J. de Smith, Mieke M. van Haelst, Richard J. Ellis, Susan Holder, Stewart J. Payne, Sugera K. Hashim, Philippe Froguel, Alexandra I. F. Blakemore,

Genetics and Neurodevelopmental Disorders

American Journal of Medical Genetics Part AVolume 155, Issue 5 p. 1192-1195 Research Letter Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems† Adam J. de Smith, Adam J. de Smith Department of Genomics of Common Disease, Imperial College London, Hammersmith Hospital Campus, London, UKSearch for more papers by this authorMieke M. van Haelst, Mieke M. van Haelst Department of Medical Genetics, University Medical Centre, Utrecht, The NetherlandsSearch for more papers by this authorRichard J. Ellis, Richard J. Ellis North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorSusan E. Holder, Susan E. Holder North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorStewart J. Payne, Stewart J. Payne North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorSugera K. Hashim, Sugera K. Hashim North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorPhilippe Froguel, Philippe Froguel Department of Genomics of Common Disease, Imperial College London, Hammersmith Hospital Campus, London, UK CNRS 8199–University of Lille Nord de France, Pasteur Institute, Lille, FranceSearch for more papers by this authorAlexandra I.F. Blakemore, Corresponding Author Alexandra I.F. Blakemore [email protected] Department of Genomics of Common Disease, Imperial College London, Hammersmith Hospital Campus, London, UKDepartment of Genomics of Common Disease, Imperial College London, Room E301 Burlington Danes Building, Du Cane Road, Hammersmith, London W12 0NN, UK.Search for more papers by this author Adam J. de Smith, Adam J. de Smith Department of Genomics of Common Disease, Imperial College London, Hammersmith Hospital Campus, London, UKSearch for more papers by this authorMieke M. van Haelst, Mieke M. van Haelst Department of Medical Genetics, University Medical Centre, Utrecht, The NetherlandsSearch for more papers by this authorRichard J. Ellis, Richard J. Ellis North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorSusan E. Holder, Susan E. Holder North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorStewart J. Payne, Stewart J. Payne North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorSugera K. Hashim, Sugera K. Hashim North West Thames Regional Genetics Service, NWLH NHS Trust, Harrow, UKSearch for more papers by this authorPhilippe Froguel, Philippe Froguel Department of Genomics of Common Disease, Imperial College London, Hammersmith Hospital Campus, London, UK CNRS 8199–University of Lille Nord de France, Pasteur Institute, Lille, FranceSearch for more papers by this authorAlexandra I.F. Blakemore, Corresponding Author Alexandra I.F. Blakemore [email protected] Department of Genomics of Common Disease, Imperial College London, Hammersmith Hospital Campus, London, UKDepartment of Genomics of Common Disease, Imperial College London, Room E301 Burlington Danes Building, Du Cane Road, Hammersmith, London W12 0NN, UK.Search for more papers by this author First published: 04 April 2011 https://doi.org/10.1002/ajmg.a.33986Citations: 18 † How to Cite this Article: de Smith AJ, van Haelst MM, Ellis RJ, Holder SE, Payne SJ, Hashim SK, Froguel P, Blakemore AIF. 2011. Chromosome 19p13.3 deletion in a patient with macrocephaly, obesity, mental retardation, and behavior problems. Am J Med Genet Part A 155:1192–1195. 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