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Page 1
Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM.
Turk Arch Pediatr. 2022 Sep;57(5):521-525. doi: 10.5152/TurkArchPediatr.2022.22070.
Turk Arch Pediatr. 2022.
PMID: 35950747
Free PMC article.
YAP/TEAD1 Complex Is a Default Repressor of Cardiac Toll-Like Receptor Genes.
Gao Y, Sun Y, Ercan-Sencicek AG, King JS, Akerberg BN, Ma Q, Kontaridis MI, Pu WT, Lin Z.
Gao Y, et al. Among authors: ercan sencicek ag.
Int J Mol Sci. 2021 Jun 22;22(13):6649. doi: 10.3390/ijms22136649.
Int J Mol Sci. 2021.
PMID: 34206257
Free PMC article.
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Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly.
Kaymakcalan H, Kaya İ, Cevher Binici N, Nikerel E, Özbaran B, Görkem Aksoy M, Erbilgin S, Özyurt G, Jahan N, Çelik D, Yararbaş K, Yalçınkaya L, Köse S, Durak S, Ercan-Sencicek AG.
Kaymakcalan H, et al. Among authors: ercan sencicek ag.
Mol Genet Genomic Med. 2021 Aug;9(8):e1739. doi: 10.1002/mgg3.1739. Epub 2021 Jul 16.
Mol Genet Genomic Med. 2021.
PMID: 34268892
Free PMC article.
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Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence?
Tüysüz B, Ercan-Sencicek AG, Canpolat N, Koparır A, Yılmaz S, Kılıçaslan I, Gülez B, Bilguvar K, Günel M.
Tüysüz B, et al. Among authors: ercan sencicek ag.
Am J Med Genet A. 2016 May;170A(5):1187-95. doi: 10.1002/ajmg.a.37543. Epub 2016 Jan 8.
Am J Med Genet A. 2016.
PMID: 26749367
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A patient with mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratodermia syndrome caused by AP1B1 gene variant.
Meriç R, Ercan-Sencicek AG, Uludağ Alkaya D, Şahin Y, Sar M, Bilguvar K, Tüysüz B.
Meriç R, et al. Among authors: ercan sencicek ag.
Clin Dysmorphol. 2021 Jan;30(1):54-57. doi: 10.1097/MCD.0000000000000350.
Clin Dysmorphol. 2021.
PMID: 32969855
No abstract available.
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Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.
Gupta AR, Pirruccello M, Cheng F, Kang HJ, Fernandez TV, Baskin JM, Choi M, Liu L, Ercan-Sencicek AG, Murdoch JD, Klei L, Neale BM, Franjic D, Daly MJ, Lifton RP, De Camilli P, Zhao H, Sestan N, State MW.
Gupta AR, et al. Among authors: ercan sencicek ag.
Mol Autism. 2014 Apr 29;5:31. doi: 10.1186/2040-2392-5-31. eCollection 2014.
Mol Autism. 2014.
PMID: 24860643
Free PMC article.
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A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family group.
Bayrakli F, Guney I, Bayri Y, Ercan-Sencicek AG, Ceyhan D, Cankaya T, Mason C, Bilguvar K, Bayrakli S, Mane SM, State MW, Gunel M.
Bayrakli F, et al. Among authors: ercan sencicek ag.
J Clin Neurosci. 2009 Dec;16(12):1610-4. doi: 10.1016/j.jocn.2009.03.022. Epub 2009 Sep 29.
J Clin Neurosci. 2009.
PMID: 19793656
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