Tuesday, January 27, 2015

Journal of Human Genetics - Table of Contents alert Volume 60 Issue 1

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Journal of Human Genetics

TABLE OF CONTENTS

Volume 60, Issue 1 (January 2015)

In this issue
Original Articles
Corrigendum

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Original Articles

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall, Şükrü Candan, Tülay Tos, İhsan Esen, Mustafa Taşkesen, Atilla Çayır, Şükrü Öztürk, İhsan Üstün, Esra Ataman, Emin Karaca, Taha Reşid Özdemir, İlknur Erol, Fehime Kara Eroğlu, Deniz Torun, Erhan Parıltay, Elif Yılmaz-Güleç, Ender Karaca, M Emre Atabek, Nursel Elçioğlu, İlhan Satman, Claes Möller, Jean Muller, Jürgen K Naggert and Rıza Köksal Özgül

J Hum Genet 2015 60: 1-9; advance online publication, October 9, 2014; 10.1038/jhg.2014.85

Abstract | Full Text

Genetic variant in NDUFS1 gene is associated with schizophrenia and negative symptoms in Han Chinese

Yunlong Zhu, Zhongliang Wang, Jianliang Ni, Yi Zhang, Meijuan Chen, Jun Cai, Xiao Li, Wen Zhang and Chen Zhang

J Hum Genet 2015 60: 11-16; advance online publication, October 30, 2014; 10.1038/jhg.2014.94

Abstract | Full Text

Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation

Milena Simioni, Tânia Kawasaki Araujo, Isabella Lopes Monlleo, Cláudia Vianna Maurer-Morelli and Vera Lúcia Gil-da-Silva-Lopes

J Hum Genet 2015 60: 17-25; advance online publication, November 13, 2014; 10.1038/jhg.2014.96

Abstract | Full Text

Identification of two novel mutations in the NOG gene associated with congenital stapes ankylosis and symphalangism

Akira Ganaha, Tadashi Kaname, Yukinori Akazawa, Teruyuki Higa, Ayano Shinjou, Kenji Naritomi and Mikio Suzuki

J Hum Genet 2015 60: 27-34; advance online publication, November 13, 2014; 10.1038/jhg.2014.97

Abstract | Full Text

Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms

Hiroko Sato, Toshihiko Uchida, Kentaro Toyota, Tomohiro Nakamura, Gen Tamiya, Miyako Kanno, Taeko Hashimoto, Masashi Watanabe, Kuraaki Aoki and Kiyoshi Hayasaka

J Hum Genet 2015 60: 35-40; advance online publication, November 13, 2014; 10.1038/jhg.2014.98

Abstract | Full Text

Sousse: extreme genetic heterogeneity in North Africa

Karima Fadhlaoui-Zid, Ralph Garcia-Bertrand, Miguel A Alfonso-Sánchez, Ramzi Zemni, Amel Benammar-Elgaaied and Rene J Herrera

J Hum Genet 2015 60: 41-49; advance online publication, December 4, 2014; 10.1038/jhg.2014.99

Abstract | Full Text

Corrigendum

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall, Şükrü Candan, Tülay Tos, İhsan Esen, Mustafa Taşkesen, Atilla Çayır, Şükrü Öztürk, İhsan Üstün, Esra Ataman, Emin Karaca, Taha Reşid Özdemir, İlknur Erol, Fehime Kara Eroğlu, Deniz Torun, Erhan Parıltay, Elif Yılmaz-Güleç, Ender Karaca, M Emre Atabek, Nursel Elçioğlu, İlhan Satman, Claes Möller, Jean Muller, Jürgen K Naggert and Rıza Köksal Özgül

J Hum Genet 2015 60: 51; 10.1038/jhg.2014.101

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