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Year | Number of Results |
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2018 | 2 |
2023 | 1 |
2024 | 1 |
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M. saeidian
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M. Saiedian
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Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.
J Inherit Metab Dis. 2018 Nov;41(6):1159-1167. doi: 10.1007/s10545-018-0228-6. Epub 2018 Aug 29.
J Inherit Metab Dis. 2018.
PMID: 30159852
High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations.
Qu HQ, Glessner JT, Qu J, Liu Y, Watson D, Chang X, Saeidian AH, Qiu H, Mentch FD, Connolly JJ, Hakonarson H.
Qu HQ, et al.
Transl Res. 2024 Apr;266:49-56. doi: 10.1016/j.trsl.2023.11.004. Epub 2023 Nov 19.
Transl Res. 2024.
PMID: 37989391
Notably, deletions involving E2F target genes and genes implicated in mitotic spindle assembly and G2/M checkpoint were identified, potentially disrupting cell-cycle progression and providing mechanistic insights into the concurrent occurrence of BDs and cancers....
Notably, deletions involving E2F target genes and genes implicated in mitotic spindle assembly and G2/M checkpoint were identified, p …
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First report of COL7A1 mutations in two patients with recessive dystrophic epidermolysis bullosa from Peru.
Saeidian AH, Youssefian L, Rosales-Solis GM, Vahidnezhad H, Atanasova VS, Uitto J, South AP, Salas-Alanis JC.
Saeidian AH, et al.
Clin Exp Dermatol. 2018 Aug;43(6):719-722. doi: 10.1111/ced.13400. Epub 2018 Feb 9.
Clin Exp Dermatol. 2018.
PMID: 29427316
No abstract available.
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