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Open Access
Peer-reviewed
Research Article
Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders
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Kagistia H. Utami,
Affiliations Human Genetics, Genome Institute of Singapore, Singapore, Singapore, Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
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Axel M. Hillmer,
Affiliation Cancer Therapeutics and Stratified Oncology, Genome Institute of Singapore, Singapore, Singapore
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Irene Aksoy,
Affiliation Stem Cells and Developmental Biology, Genome Institute of Singapore, Singapore, Singapore
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Elaine G. Y. Chew,
Affiliation Cancer Therapeutics and Stratified Oncology, Genome Institute of Singapore, Singapore, Singapore
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Audrey S. M. Teo,
Affiliation Cancer Therapeutics and Stratified Oncology, Genome Institute of Singapore, Singapore, Singapore
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Zhenshui Zhang,
Affiliation Cancer Therapeutics and Stratified Oncology, Genome Institute of Singapore, Singapore, Singapore
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Charlie W. H. Lee,
Affiliation Computational and Mathematical Biology, Genome Institute of Singapore, Singapore, Singapore
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Pauline J. Chen,
Affiliation Computational and Mathematical Biology, Genome Institute of Singapore, Singapore, Singapore
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Chan Chee Seng,
Affiliation Scientific & Research Computing, Genome Institute of Singapore, Singapore, Singapore
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Pramila N. Ariyaratne,
Affiliation Computational and Mathematical Biology, Genome Institute of Singapore, Singapore, Singapore
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Sigrid L. Rouam,
Affiliation Computational and Mathematical Biology, Genome Institute of Singapore, Singapore, Singapore
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Lim Seong Soo,
Affiliation Human Genetics, Genome Institute of Singapore, Singapore, Singapore
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Saira Yousoof,
Affiliations Eye and Developmental Genetics Research, The Children’s Hospital at Westmead, Children’s Medical Research Institute and Save Sight Institute, Sydney, New South Wales, Australia, Disciplines of Paediatrics and Child Health and Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia
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Ivan Prokudin,
Affiliations Eye and Developmental Genetics Research, The Children’s Hospital at Westmead, Children’s Medical Research Institute and Save Sight Institute, Sydney, New South Wales, Australia, Disciplines of Paediatrics and Child Health and Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia
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Gregory Peters,
Affiliation Department of Cytogenetics, The Children’s Hospital at Westmead, Sydney, New South Wales, Australia
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Felicity Collins,
Affiliation Department of Clinical Genetics, The Children’s Hospital at Westmead, Sydney, New South Wales, Australia
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Meredith Wilson,
Affiliation Department of Clinical Genetics, The Children’s Hospital at Westmead, Sydney, New South Wales, Australia
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Alyson Kakakios,
Affiliation Department of Immunology, The Children’s Hospital at Westmead, Sydney, New South Wales, Australia
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Georges Haddad,
Affiliation Unité de Génétique, Centre Hospitalier, Blois, France
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Arnaud Menuet,
Affiliation Service de Genetique INEM UMR7355 CNRS-University, Centre Hospitalier Régional d’Orléans, Orléans, France
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Olivier Perche,
Affiliation Service de Genetique INEM UMR7355 CNRS-University, Centre Hospitalier Régional d’Orléans, Orléans, France
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Stacey Kiat Hong Tay,
Affiliation Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
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Ken W. K. Sung,
Affiliation Computational and Mathematical Biology, Genome Institute of Singapore, Singapore, Singapore
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Xiaoan Ruan,
Affiliation Genome Technology and Biology, Genome Institute of Singapore, Singapore, Singapore
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Yijun Ruan,
Affiliation Genome Technology and Biology, Genome Institute of Singapore, Singapore, Singapore
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Edison T. Liu,
Affiliation Cancer Therapeutics and Stratified Oncology, Genome Institute of Singapore, Singapore, Singapore
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Sylvain Briault,
Affiliation Service de Genetique INEM UMR7355 CNRS-University, Centre Hospitalier Régional d’Orléans, Orléans, France
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Robyn V. Jamieson,
Affiliation Eye and Developmental Genetics Research, The Children’s Hospital at Westmead, Children’s Medical Research Institute and Save Sight Institute, Sydney, New South Wales, Australia
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Sonia Davila,
Affiliation Human Genetics, Genome Institute of Singapore, Singapore, Singapore
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Valere Cacheux
* E-mail: valerecacheux@gmail.com
Affiliation Human Genetics, Genome Institute of Singapore, Singapore, Singapore
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Detection of Chromosomal Breakpoints in Patients with Developmental Delay and Speech Disorders
- Kagistia H. Utami,
- Axel M. Hillmer,
- Irene Aksoy,
- Elaine G. Y. Chew,
- Audrey S. M. Teo,
- Zhenshui Zhang,
- Charlie W. H. Lee,
- Pauline J. Chen,
- Chan Chee Seng,
- Pramila N. Ariyaratne
- Published: March 6, 2014
- https://doi.org/10.1371/journal.pone.0090852