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Journal Article

Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations

MPS-Authors
http://pubman.mpdl.mpg.de/cone/persons/resource/persons50163

Garshasbi,  M.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons50051

Moheb,  L. A.
Familial Cognitive Disorders (Luciana Musante), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons50501

Ropers,  H.-H.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Fulltext (public)

Papari.pdf
(Publisher version), 610KB

Supplementary Material (public)
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Citation

Papari, E., Bastami, M., Farhadi, A., Abedini, S., Hosseini, M., Bahman, I., et al. (2013). Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations. Clinical Genetics: an international journal of genetics in medicine, 83(5), 488-490. doi:10.1111/j.1399-0004.2012.01949.x.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-EC7C-9
Abstract
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