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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 novel mutation in MCPH1 gene in an Iranian family with primary microcephaly.
Hosseini MM, Tonekaboni SH, Papari E, Bahman I, Behjati F, Kahrizi K, Najmabadi H.
Hosseini MM, et al. Among authors: papari e.
J Pak Med Assoc. 2012 Nov;62(11):1244-7.
J Pak Med Assoc. 2012.
PMID: 23866422
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Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations.
Papari E, Bastami M, Farhadi A, Abedini SS, Hosseini M, Bahman I, Mohseni M, Garshasbi M, Moheb LA, Behjati F, Kahrizi K, Ropers HH, Najmabadi H.
Papari E, et al.
Clin Genet. 2013 May;83(5):488-90. doi: 10.1111/j.1399-0004.2012.01949.x. Epub 2012 Sep 18.
Clin Genet. 2013.
PMID: 22989186
No abstract available.
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Identification of candidate microRNA markers of endometriosis with the use of next-generation sequencing and quantitative real-time polymerase chain reaction.
Papari E, Noruzinia M, Kashani L, Foster WG.
Papari E, et al.
Fertil Steril. 2020 Jun;113(6):1232-1241. doi: 10.1016/j.fertnstert.2020.01.026.
Fertil Steril. 2020.
PMID: 32482255
Free article.
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A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability.
Larti F, Kahrizi K, Musante L, Hu H, Papari E, Fattahi Z, Bazazzadegan N, Liu Z, Banan M, Garshasbi M, Wienker TF, Hilger Ropers H, Galjart N, Najmabadi H.
Larti F, et al. Among authors: papari e.
Eur J Hum Genet. 2015 Mar;23(3):416. doi: 10.1038/ejhg.2014.152.
Eur J Hum Genet. 2015.
PMID: 25672248
Free PMC article.
No abstract available.
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A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability.
Larti F, Kahrizi K, Musante L, Hu H, Papari E, Fattahi Z, Bazazzadegan N, Liu Z, Banan M, Garshasbi M, Wienker TF, Ropers HH, Galjart N, Najmabadi H.
Larti F, et al. Among authors: papari e.
Eur J Hum Genet. 2015 Mar;23(3):331-6. doi: 10.1038/ejhg.2014.13. Epub 2014 Feb 26.
Eur J Hum Genet. 2015.
PMID: 24569606
Free PMC article.
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