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Publisher: Wiley-Blackwell

Volume 83, Number 1, 1 January 2019

Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss
pp. 1-10(10)
Authors: Azadegan‐Dehkordi, Fatemeh; Ahmadi, Reza; Koohiyan, Mahbobeh; Hashemzadeh‐Chaleshtori, Morteza

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Adaptation to milking agropastoralism in Chilean goat herders and nutritional benefit of lactase persistence
pp. 11-22(12)
Authors: Montalva, Nicolás; Adhikari, Kaustubh; Liebert, Anke; Mendoza‐Revilla, Javier; Flores, Sergio V.; Mace, Ruth; Swallow, Dallas M.

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The rs2516839 variation of USF1 gene is associated with 4‐year mortality of nonagenarian women: The Vitality 90+ study
pp. 34-45(12)
Authors: Ozsait‐Selcuk, B.; Komurcu‐Bayrak, E.; Jylhä, M.; Luukkaala, T.; Perola, M.; Kristiansson, K.; Mononen, N.; Hurme, M.; Kähönen, M.; Goebeler, S.; Laaksonen, R.; Hervonen, A.; Erginel‐Unaltuna, N.; Karhunen, P.J.; Lehtimäki, T.

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A PEAR1 polymorphism (rs12041331) is associated with risk of coronary artery aneurysm in Kawasaki disease
pp. 54-62(9)
Authors: Pi, Lei; Xu, Yufen; Fu, Lanyan; Zhang, Li; Liu, Yunfeng; Zhou, Huazhong; Che, Di; Gu, Xiaoqiong

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Association of polymorphisms in genes coding for antioxidant enzymes and human male infertility
pp. 63-72(10)
Authors: García Rodríguez, Anaís; la Casa, Moises; Johnston, Stephen; Gosálvez, Jaime; Roy, Rosa

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