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FEN1 −69G>A and +4150G>T polymorphisms and breast cancer risk
Rezaei, Maryam, Hashemi, Mohammad, Sanaei, Sara, Mashhadi, Mohammad Ali, Hashemi, Seyed Mehdi, Bahari, Gholamreza, Taheri, Mohsen
Published in Biomedical reports (01.10.2016)
Published in Biomedical reports (01.10.2016)
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Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder
Hamedani, Shima Yazdandoost, Gharesouran, Jalal, Noroozi, Rezvan, Sayad, Arezou, Omrani, Mir Davood, Mir, Atefeh, Afjeh, Sarah Sadat Aghabozrg, Toghi, Mehdi, Manoochehrabadi, Saba, Ghafouri-Fard, Soudeh, Taheri, Mohammad
Published in Metabolic brain disease (01.06.2017)
Published in Metabolic brain disease (01.06.2017)
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Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies
Sivadorai, P, Cherninkova, S, Bouwer, S, Kamenarova, K, Angelicheva, D, Seeman, P, Hollingsworth, K, Mihaylova, V, Oscar, A, Dimitrova, G, Kaneva, R, Tournev, I, Kalaydjieva, L
Published in Clinical genetics (01.07.2008)
Published in Clinical genetics (01.07.2008)
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IGF2BP2 polymorphisms as genetic biomarkers for either schizophrenia or type 2 diabetes mellitus: A case-control study
Sargazi, Saman, Heidari Nia, Milad, Saravani, Ramin, Jafari Shahroudi, Mahdieh, Jahantigh, Danial, Shakiba, Mansoor
Published in Gene reports (01.09.2020)
Published in Gene reports (01.09.2020)
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Differential expression profiling between the relative normal and dystrophic muscle tissues from the same LGMD patient
Zhang, Yong, Ye, Jianwei, Chen, Dazhi, Zhao, Xinyi, Xiao, Xingjun, Tai, Sheng, Yang, Wei, Zhu, Dahai
Published in Journal of translational medicine (19.12.2006)
Published in Journal of translational medicine (19.12.2006)
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A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect
Di Maria, E, Gulli, R, Balestra, P, Cassandrini, D, Pigullo, S, Doria-Lamba, L, Bado, M, Schenone, A, Ajmar, F, Mandich, P, Bellone, E
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2004)
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2004)
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Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype
Chong, Belinda, Hegde, Madhuri, Fawkner, Matthew, Simonet, Scott, Cassinelli, Hamilton, Coker, Mahmut, Kanis, John, Seidel, Joerg, Tau, Cristina, Tüysüz, Beyhan, Yüksel, Bilgin, Love, Donald, Cundy, Tim
Published in Journal of bone and mineral research (01.12.2003)
Published in Journal of bone and mineral research (01.12.2003)
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Genetic Diagnosis via Whole Exome Sequencing in Taiwanese Patients with Hypertriglyceridemia
Chiou, Kuan-Rau, Chen, Chung-Yung, Charng, Min-ji
Published in Journal of Atherosclerosis and Thrombosis (01.01.2015)
Published in Journal of Atherosclerosis and Thrombosis (01.01.2015)
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Study of association between pre-senile cataracts and rs11615 of ERCC1 , rs13181 of ERCC2 , and rs25487 of XRCC1 polymorphisms in a Spanish population
López-Valverde, Gloria, Garcia-Martin, Elena, Fernández-Mateos, Javier, Cruz-González, Fernando, Larrosa-Povés, José M., Polo-Llorens, Vicente, Pablo-Júlvez, Luis E., González-Sarmiento, Rogelio
Published in Ophthalmic genetics (04.07.2017)
Published in Ophthalmic genetics (04.07.2017)
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Familial Risks for Hospitalization with Endocrine Diseases
Hemminki, Kari, Shu, Xiaochen, Li, Xinjun, Ji, Jianguang, Sundquist, Jan, Sundquist, Kristina
Published in The journal of clinical endocrinology and metabolism (01.12.2008)
Published in The journal of clinical endocrinology and metabolism (01.12.2008)
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Recurrent mutation in CDMP1 in a family with Grebe chondrodysplasia: broadening the phenotypic manifestation of syndrome in Pakistani population
Mumtaz, Sara, Riaz, Hafiza Fizzah, Touseef, Mohammad, Basit, Sulman, Faiyaz Ul Haque, Muhammad, Malik, Sajid
Published in Pakistan journal of medical sciences (31.12.2015)
Published in Pakistan journal of medical sciences (31.12.2015)
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Sepiapterin reductase deficiency: a congenital dopa-responsive motor and cognitive disorder
Neville, B. G. R., Parascandalo, R., Farrugia, R., Felice, A.
Published in Brain (London, England : 1878) (01.10.2005)
Published in Brain (London, England : 1878) (01.10.2005)
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Familial abdominal aortic aneurysms: Collection of 233 multiplex families
Kuivaniemi, Helena, Shibamura, Hidenori, Arthur, Claudette, Berguer, Ramon, Cole, C.William, Juvonen, Tatu, Kline, Ronald A., Limet, Raymond, MacKean, Gerry, Norrgård, Örjan, Pals, Gerard, Powell, Janet T., Rainio, Pekka, Sakalihasan, Natzi, van Vlijmen-van Keulen, Clarissa, Verloes, Alain, Tromp, Gerard
Published in Journal of vascular surgery (01.02.2003)
Published in Journal of vascular surgery (01.02.2003)
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