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Publisher: Wiley-Blackwell

Volume 79, Number 3, 1 May 2015

Free Content Founder Haplotype Analysis of Fanconi Anemia in the Korean Population Finds Common Ancestral Haplotypes for a FANCG Variant
pp. 153-161(9)
Authors: Park, Joonhong; Kim, Myungshin; Jang, Woori; Chae, Hyojin; Kim, Yonggoo; Chung, Nack‐Gyun; Lee, Jae‐Wook; Cho, Bin; Jeong, Dae‐Chul; Park, In Yang; Park, Mi Sun

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Free Content Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria
pp. 162-172(11)
Authors: Gonzaga, Ana Denise Gomes; Amorim, Lidia Maria da Fonte; Fonseca, Ana Beatriz Monteiro; Nogueira, Tatiana Lucia Santos; Pereira, Olga Maria Diniz; Nagai, Maria Aparecida; Oliveira Barretto, Orlando Cesar; Ribeiro, Georgina Severo

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Free Content Association of Monocyte Chemoattractant Protein‐1 (MCP‐1)‐2518A>G Polymorphism with Susceptibility to Coronary Artery Disease: A Meta‐Analysis
pp. 173-187(15)
Authors: Bai, Xiao‐Yan; Li, Shujing; Wang, Miao; Qu, Xinjian; Hu, Gaolei; Xu, Zhaowei; Chen, Min; He, Guo‐Wei; Wu, Huijian

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Free Content Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans
pp. 188-198(11)
Authors: Levran, Orna; Randesi, Matthew; Rosa, Joel Correa; Ott, Jurg; Rotrosen, John; Adelson, Miriam; Kreek, Mary Jeanne

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Free Content Kullback–Leibler Distance Methods for Detecting Disease Association with Rare Variants from Sequencing Data
pp. 199-208(10)
Authors: Turkmen, Asuman S.; Yan, Zhifei; Hu, Yue‐Qing; Lin, Shili

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Free Content Early Myoclonic Encephalopathy in 9q33‐q34 Deletion Encompassing STXBP1 and SPTAN1
pp. 209-217(9)
Authors: Nicita, Francesco; Ulgiati, Fiorenza; Bernardini, Laura; Garone, Giacomo; Papetti, Laura; Novelli, Antonio; Spalice, Alberto

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Free Content A Novel TAZ Gene Mutation and Mosaicism in a Polish Family with Barth Syndrome
pp. 218-224(7)
Authors: Zapała, Barbara; Płatek, Teresa; Wybrańska, Iwona

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