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Research description

"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes.
Rafati M, Seyyedaboutorabi E, Ghadirzadeh M, Heshmati Y, Adibi H, Keihanidoust Z, et al
Mol Cytogenet 2012 Jan;5(1):9

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements.
Rafati M, Ghadirzadeh M, Heshmati Y, Adibi H, Keihanidoust Z, Eshraghian M, et al
Mol Cytogenet 2012 Jan;5(1):4

Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease.
Zarif Yeganeh M, Mirabzadeh A, Khorram Khorshid H, Kamali K, Heshmati Y, Gozalpour E, et al
Am. J. Med. Genet. B Neuropsychiatr. Genet. 2010 Jan;153B(1):347-9

A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin-1 gene and risk of Alzheimer's disease; extra-short alleles and accumulated allele homozygosity.
Heshmati Y, Mirabzadeh A, Feizzade G, Gilanipour M, Etminan M, Khoram Khorshid H, et al
Am. J. Med. Genet. B Neuropsychiatr. Genet. 2009 Mar;150B(2):248-53

Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome.
Moheb L, Tzschach A, Garshasbi M, Kahrizi K, Darvish H, Heshmati Y, et al
Eur. J. Hum. Genet. 2008 Feb;16(2):270-3

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