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Genetics of intellectual disability in consanguineous families.
Mol Psychiatry. 2019 Jul;24(7):1027-1039. doi: 10.1038/s41380-017-0012-2. Epub 2018 Jan 4.
Mol Psychiatry. 2019.
PMID: 29302074
A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.
Darvish H, Esmaeeli-Nieh S, Monajemi GB, Mohseni M, Ghasemi-Firouzabadi S, Abedini SS, Bahman I, Jamali P, Azimi S, Mojahedi F, Dehghan A, Shafeghati Y, Jankhah A, Falah M, Soltani Banavandi MJ, Ghani M, Garshasbi M, Rakhshani F, Naghavi A, Tzschach A, Neitzel H, Ropers HH, Kuss AW, Behjati F, Kahrizi K, Najmabadi H.
Darvish H, et al. Among authors: soltani banavandi mj.
J Med Genet. 2010 Dec;47(12):823-8. doi: 10.1136/jmg.2009.076398. Epub 2010 Oct 26.
J Med Genet. 2010.
PMID: 20978018
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Investigation of genetic causes of intellectual disability in kerman province, South East of iran.
Soltani Banavandi MJ, Kahrizi K, Behjati F, Mohseni M, Darvish H, Bahman I, Abedinni SS, Ghasemi Firouzabadi S, Jafari E, Ghadami Sh, Sabbagh F, Kavoosi GR, Najmabadi H.
Soltani Banavandi MJ, et al.
Iran Red Crescent Med J. 2012 Feb;14(2):79-85. Epub 2012 Feb 1.
Iran Red Crescent Med J. 2012.
PMID: 22737560
Free PMC article.
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Association between VKORC1 gene polymorphism and warfarin dose requirement and frequency of VKORC1 gene polymorphism in patients from Kerman province.
Soltani Banavandi MJ, Satarzadeh N.
Soltani Banavandi MJ, et al.
Pharmacogenomics J. 2020 Aug;20(4):574-578. doi: 10.1038/s41397-019-0146-5. Epub 2020 Jan 6.
Pharmacogenomics J. 2020.
PMID: 31902949
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