Ala-Mello Sirpa
Research Subjects
Ala-Mello Sirpa has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Esa Kuusinen
Department of Pediatrics, Satakunta Hospital District, Pori, Finland.
2 shared publications - Ilari Scheinin
Department of Pathology, Haartman Institute, University of Helsinki, and Laboratory of Helsinki and Uusimaa University Hospital, Helsinki, Finland.
2 shared publications - Janna Saarela
Institute for Molecular Medicine Finland, HiLIFE, University of Helsinki, Helsinki, Finland
2 shared publications - Kati Kristiansson
Department of Public Health and Welfare, Finnish Institute for Health and Welfare, Helsinki, Finland
2 shared publications - Kristiina Avela
Väestöliitto, The Family Federation of Finland, Department of Medical Genetics, Helsinki, Finland
2 shared publications - Lahermo Päivi
Institute for Molecular Medicine Finland FIMM, University Helsinki, Helsinki, Finland.
2 shared publications
Latest Publications
- Open Access
- 18 November 2014
- Published by Springer Nature in BMC Medical Genetics
- Vol. 15 (1) , 124
Erratum to: high-resolution SNP array analysis of patients with developmental disorder and normal array CGH result
- 18 November 2014
- Published by Springer Nature in BMC Medical Genetics
- Vol. 15 (1) , 124
Open AccessErratum to: high-resolution SNP array analysis of patients with developmental disorder and normal array CGH result
- Open Access
- 18 September 2012
- Published by Springer Nature in BMC Medical Genetics
- Vol. 13 (1) , 84
High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results
Diagnostic analysis of patients with developmental disorders has improved over recent years largely due to the use of microarray technology. Array methods that facilitate copy number analysis have enabled the diagnosis of up to 20% more patients with previously normal karyotyping results. A substantial number of patients remain undiagnosed, however.
- 18 September 2012
- Published by Springer Nature in BMC Medical Genetics
- Vol. 13 (1) , 84
Open AccessHigh-resolution SNP array analysis of patients with developmental disorder and normal array CGH results
Diagnostic analysis of patients with developmental disorders has improved over recent years largely due to the use of microarray technology. Array methods that facilitate copy number analysis have enabled the diagnosis of up to 20% more patients with previously normal karyotyping results. A substantial number of patients remain undiagnosed, however.