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Publisher: Wiley-Blackwell

Volume 82, Number 6, 1 November 2018

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Association of CTLA‐4 polymorphisms with increased risks of myasthenia gravis
pp. 358-369(12)
Authors: Li, Fang; Yuan, Wuzhou; Wu, Xiushan

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The association of LRP6 rs2302685 (V1062I) polymorphism with the risk of hyperlipidemia in Iranian children and adolescents
pp. 382-388(7)
Authors: Montazeri‐Najafabady, Nima; Dabbaghmanesh, Mohammad Hossein; Mohammadian Amiri, Rajeeh

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Polymorphisms of dopamine receptor genes DRD2 and DRD4 in African populations of Hadza and Datoga differing in the level of culturally permitted aggression
pp. 407-414(8)
Authors: Sukhodolskaya, Evgeniya M.; Fehretdinova, Daniya I.; Shibalev, Dmitry V.; Lazebny, Oleg E.; Mabulla, Audax Z. P.; Butovskaya, Marina L.; Ryskov, Alexey P.; Vasilyev, Vasily V.

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CHRNA3 rs1051730 and CHRNA5 rs16969968 polymorphisms are associated with heavy smoking, lung cancer, and chronic obstructive pulmonary disease in a mexican population
pp. 415-424(10)
Authors: Pérez‐Morales, Rebeca; González‐Zamora, Alberto; González‐Delgado, María Fernanda; Calleros Rincón, Esperanza Y.; Olivas Calderón, Edgar H.; Martínez‐Ramírez, Ollin Celeste; Rubio, Julieta

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Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients
pp. 425-436(12)
Authors: Palma Milla, Carmen; Lezana Rosales, José Miguel; López Montiel, Javier; Andrés Garrido, Lucas David; Sánchez Linares, Carlos; Carmona Tamajón, Sandra; Torres Fernández, Carmen; Sánchez González, Pablo; Franco Freire, Sara; Benito López, Carmen; López Siles, Juan

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Analysis of causal effect of APOA5 variants on premature coronary artery disease
pp. 437-447(11)
Authors: Wang, Fan; Wang, Isabel Z.; Ellis, Stephen; Archacki, Stephen; Barnard, John; Hubbard, Carlos; Topol, Eric J.; Chen, Qiuyun; Wang, Qing K.

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Genetic susceptibility of glutathione S‐transferase genes (GSTM1/T1 and P1) to coronary artery disease in Asian Indians
pp. 448-456(9)
Authors: Bhatti, J. S.; Vijayvergiya, R.; Singh, B.; Bhatti, G. K.

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Potential dysfunctional effects of synonymous variants: Insights from an exhaustive in silico analysis of the ABCB4 gene
pp. 457-468(12)
Authors: Khabou, Boudour; Tabebi, Mouna; Siala‐Sahnoun, Olfa; Mkaouar‐Rebai, Emna; Rebai, Ahmed; Fakhfakh, Faiza

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Genotype–phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams‐Beuren syndrome
pp. 469-476(8)
Authors: Ghaffari, Mahsa; Tahmasebi Birgani, Maryam; Kariminejad, Roxana; Saberi, Alihossein

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Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta
pp. 477-481(5)
Authors: Rodriguez Celin, Mercedes; Moosa, Shahida; Fano, Virginia

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Deletion at 12q12 increases the risk of developmental delay and intellectual disability
pp. 482-487(6)
Authors: Weng, Ying; Luo, Xiaoping; Hou, Ling

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