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

Papari, E.; Bastami, M.; Farhadi, A.; Abedini, S.; Hosseini, M.; Bahman, I.; Mohseni, M.; Garshasbi, M.; Moheb, L. A.; Behjati, F.; Kahrizi, K.; Ropers, H.-H.; Najmabadi, H.

doi:10.1111/j.1399-0004.2012.01949.x

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

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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;

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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;

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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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引用

Papari, E., Bastami, M., Farhadi, A., Abedini, S., Hosseini, M., Bahman, I., Mohseni, M., Garshasbi, M., Moheb, L. A., Behjati, F., Kahrizi, K., Ropers, H.-H., & Najmabadi, H. (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.

引用: https://hdl.handle.net/11858/00-001M-0000-000E-EC7C-9

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