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Diagnosis of genetic abnormalities in developmentally delayed patients: A new strategy combining MLPA and array‐CGH
Author(s) -
Kriek Marjolein,
Knijnenburg Jeroen,
White Stefan J.,
Rosenberg Carla,
den Dunnen Johan T.,
van Ommen GertJan B.,
Tanke Hans J.,
Breuning Martijn H.,
Szuhai Karoly
Publication year - 2007
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.31593
Subject(s) - multiplex ligation dependent probe amplification , comparative genomic hybridization , multiplex , copy number analysis , copy number variation , biology , genetics , fluorescence in situ hybridization , gene duplication , computational biology , genome , gene , chromosome , exon
Marjolein Kriek,* Jeroen Knijnenburg, Stefan J. White, Carla Rosenberg, Johan T. den Dunnen, Gert-Jan B. van Ommen, Hans J. Tanke, Martijn H. Breuning, and Karoly Szuhai Center for Human and Clinical Genetics, Leiden University Medical Center, RC Leiden, The Netherlands Department Molecular Cell Biology, Leiden University Medical Center, RC Leiden, The Netherlands Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil