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Year | Number of Results |
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2015 | 2 |
2018 | 2 |
2023 | 1 |
2024 | 1 |
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Page 1
Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia.
Adv Biomed Res. 2015 Aug 31;4:189. doi: 10.4103/2277-9175.164009. eCollection 2015.
Adv Biomed Res. 2015.
PMID: 26605228
Free PMC article.
Review.
The Effect of Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism on the Severity and Death Rate of COVID-19 in Iranian Patients.
Samet M, Yazdi M, Tajamolian M, Beygi M, Sheikhha MH, Hoseini SM.
Samet M, et al. Among authors: tajamolian m.
Biochem Genet. 2023 Dec 25. doi: 10.1007/s10528-023-10614-3. Online ahead of print.
Biochem Genet. 2023.
PMID: 38145438
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The association of RBX1 and BAMBI gene expression with oocyte maturation in PCOS women.
Monshizadeh K, Tajamolian M, Anbari F, Mehrjardi MYV, Kalantar SM, Dehghani M.
Monshizadeh K, et al. Among authors: tajamolian m.
BMC Med Genomics. 2024 Jan 18;17(1):24. doi: 10.1186/s12920-024-01800-2.
BMC Med Genomics. 2024.
PMID: 38238750
Free PMC article.
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The rs3917779 polymorphism of P-selectin's significant association with proliferative diabetic retinopathy in Yazd, Iran.
Kolahdouz P, Farashahi Yazd E, Tajamolian M, Manaviat MR, Sheikhha MH.
Kolahdouz P, et al. Among authors: tajamolian m.
Graefes Arch Clin Exp Ophthalmol. 2015 Nov;253(11):1967-72. doi: 10.1007/s00417-015-3141-9. Epub 2015 Sep 7.
Graefes Arch Clin Exp Ophthalmol. 2015.
PMID: 26344728
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A Rare Missense Mutation and a Polymorphism with High Frequency in LDLR Gene among Iranian Patients with Familial Hypercholesterolemia.
Tajamolian M, Kolahdouz P, Nikpour P, Forouzannia SK, Sheikhha MH, Yazd EF.
Tajamolian M, et al.
Adv Biomed Res. 2018 Feb 21;7:37. doi: 10.4103/2277-9175.225927. eCollection 2018.
Adv Biomed Res. 2018.
PMID: 29531935
Free PMC article.
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Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity.
Dehghani MR, Mehrjardi MYV, Dilaver N, Tajamolian M, Enayati S, Ebrahimi P, Amoli MM, Farooqi S, Maroofian R.
Dehghani MR, et al. Among authors: tajamolian m.
Eur J Med Genet. 2018 Aug;61(8):465-467. doi: 10.1016/j.ejmg.2018.03.006. Epub 2018 Mar 12.
Eur J Med Genet. 2018.
PMID: 29545012
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