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Publisher: Wiley-Blackwell

Volume 78, Number 6, 1 November 2014

Free Content Identification of Four Novel PCDH19 Mutations and Prediction of Their Functional Impact
pp. 389-398(10)
Authors: Leonardi, Emanuela; Sartori, Stefano; Vecchi, Marilena; Bettella, Elisa; Polli, Roberta; Palma, Luca De; Boniver, Clementina; Murgia, Alessandra

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Free Content The Frequency and the Effects of 21‐Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients
pp. 399-409(11)
Authors: Kirac, Deniz; Guney, Ahmet Ilter; Akcay, Teoman; Guran, Tulay; Ulucan, Korkut; Turan, Serap; Ergec, Deniz; Koc, Gulsah; Eren, Fatih; Kaspar, Elif Cigdem; Bereket, Abdullah

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Free Content Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family
pp. 410-423(14)
Authors: Cheng, Jing; Zhou, Xueya; Lu, Yu; Chen, Jing; Han, Bing; Zhu, Yuhua; Liu, Liyang; Choy, Kwong‐Wai; Han, Dongyi; Sham, Pak C.; Zhang, Michael Q.; Zhang, Xuegong; Yuan, Huijun

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Free Content Renal Agenesis in Kallmann Syndrome: A Network Approach
pp. 424-433(10)
Authors: Tickotsky, Nili; Moskovitz, Moti

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Free Content Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP‐2
pp. 434-451(18)
Authors: Menzel, Stephan; Rooks, Helen; Zelenika, Diana; Mtatiro, Siana N.; Gnanakulasekaran, Akshala; Drasar, Emma; Cox, Sharon; Liu, Li; Masood, Mariam; Silver, Nicholas; Garner, Chad; Vasavda, Nisha; Howard, Jo; Makani, Julie; Adekile, Adekunle; Pace, Betty; Spector, Tim; Farrall, Martin; Lathrop, Mark; Thein, Swee Lay

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Free Content Whole‐Genome Analyses of Lung Function, Height and Smoking
pp. 452-467(16)
Authors: Janss, Luc; Sigsgaard, Torben; Sorensen, Daniel

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Free Content Worldwide FST Estimates Relative to Five Continental‐Scale Populations
pp. 468-477(10)
Authors: Steele, Christopher D.; Court, Denise Syndercombe; Balding, David J.

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Free Content Pathway‐Guided Identification of Gene‐Gene Interactions
pp. 478-491(14)
Authors: Wang, Xin; Zhang, Daowen; Tzeng, Jung‐Ying

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