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Publisher: Wiley-Blackwell

Volume 82, Number 1, 1 January 2018

Evaluation of a Role for NPY and NPY2R in the Pathogenesis of Obesity by Mutation and Copy Number Variation Analysis in Obese Children and Adolescents
pp. 1-10(10)
Authors: Aerts, Evi; Geets, Ellen; Sorber, Laure; Beckers, Sigri; Verrijken, An; Massa, Guy; Hoorenbeeck, Kim; Verhulst, Stijn L; Gaal, Luc F; Hul, Wim

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Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family
pp. 23-34(12)
Authors: Sampaio‐Silva, Juliana; Batissoco, Ana Carla; Jesus‐Santos, Rafaela; Abath‐Neto, Osório; Scarpelli, Luciano Cesar; Nishimura, Patricia Yoshie; Galindo, Layla Testa; Bento, Ricardo Ferreira; Oiticica, Jeanne; Lezirovitz, Karina

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Single‐center experience of N‐linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs
pp. 35-47(13)
Authors: Bastaki, Fatma; Bizzari, Sami; Hamici, Sana; Nair, Pratibha; Mohamed, Madiha; Saif, Fatima; Malik, Ethar Mustafa; Al‐Ali, Mahmoud Taleb; Hamzeh, Abdul Rezzak

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Choledochal Cyst with 17q12 Chromosomal Duplication
pp. 48-51(4)
Authors: Kotalova, Radana; Dusatkova, Petra; Drabova, Jana; Elblova, Lenka; Dedic, Tomas; Cinek, Ondrej; Lebl, Jan; Pruhova, Stepanka

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Corrigendum
pp. 52-52(1)

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