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Genetic epidemiology, prevalence, and genotype–phenotype correlations in the Swedish population with osteogenesis imperfecta av Katarina Lindahl, Eva Åström, Carl‐Johan Rubin, Giedre Grigelioniené, B. Malmgren, Östen Ljunggren, Andreas Kindmark

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A cross‐sectional multicenter study of osteogenesis imperfecta in North America – results from the linked clinical research centers av Ruchita Patel, Sandesh C.S. Nagamani, David Cuthbertson, Philippe M. Campeau, J. Krischer, Jay R. Shapiro, Robert D. Steiner, Peter A. Smith, Michael B. Bober, Peter H. Byers, Melanie Pepin, Michaela Durigova, Francis H. Glorieux, Frank Rauch, B.H. Lee, Tracy Hart, V. Reid Sutton

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Astacin proteases cleave dentin sialophosphoprotein (Dspp) to generate dentin phosphoprotein (Dpp) av Shuhei Tsuchiya, James P. Simmer, Jan C.‐C. Hu, Amelia S. Richardson, Fumiko Yamakoshi, Yasuo Yamakoshi

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Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification av Muriel De La Dure‐Molla, Benjamin Fournier, Ariane Berdal

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Current and emerging treatments for the management of osteogenesis imperfecta av Franco Antoniazzi

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Heterogeneity of osteogenesis imperfecta type I. av C R Paterson, Susan J. McAllion, R Miller

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Avaliação clínica, radiográfica e laboratorial de pacientes com osteogênese imperfeita av Cláudio Santili, Miguel Akkari, Gilberto Waisberg, José Olympio Catão Bastos Júnior, William Martins Ferreira

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Genetic evidence for key roles of decorin and biglycan in dentin mineralization av Naoto Haruyama, Taduru Sreenath, Shigeki Suzuki, Xiaomei Yao, Zhigang Wang, Yong Wang, Cherlita Honeycutt, Renato V. Iozzo, Marian F. Young, Ashok B. Kulkarni

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Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome av James O’Sullivan, Carolina Cavalcante Bitu, Sarah B. Daly, Jill Urquhart, Martin Barron, Sanjeev S. Bhaskar, Hercílio Martelli‐Júnior, Pedro Eleutério dos Santos Neto, M. Adela Mansilla, Jeffrey C. Murray, Ricardo D. Coletta, Graeme Black, Michael J. Dixon

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Phenotype Characterization and DSPP Mutational Analysis of Three Brazilian Dentinogenesis Imperfecta Type II Families av Ana Carolina Acevedo, L.J.S. Santos, Lílian Marly de Paula, Juan Dong, Mary MacDougall

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COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta av Katarina Lindahl, Aileen M. Barnes, Nadja Fratzl‐Zelman, Michael P. Whyte, Theresa E. Hefferan, Elena Makareeva, Marina Brusel, Michael J. Yaszemski, Carl‐Johan Rubin, Andreas Kindmark, Paul Roschger, Klaus Klaushofer, William H. McAlister, Steven Mumm, Sergey Leikin, Efrat Kessler, Adele L. Boskey, Östen Ljunggren, Joan C. Marini

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Dentinogenesis and Dentin Sialophosphoprotein (DSPP). av Yasuo Yamakoshi

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Human tooth culture: A study model for reparative dentinogenesis and direct pulp capping materials biocompatibility av Odile Téclès, Patrick Laurent, Virginie Aubut, Imad About

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Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and... av Angelo Karunaratne, Christopher R Esapa, Jennifer Hiller, A. Boyde, Rosie Head, J. H. Duncan Bassett, Nicholas J. Terrill, Graham R. Williams, Matthew A. Brown, Peter I. Croucher, Steve D. M. Brown, Roger Cox, Asa H. Barber, Rajesh V. Thakker, Himadri S. Gupta

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A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta av Clara Barbirato, Márcio G. Almeida, M. Milanez, V. Sipolatti, Maria R. G. O. Rebouças, Ahmad Akel, V.R.R. Nunes, A.M.S. Perrone, Mayana Zatz, Iúri Drumond Louro, Flavia Paula

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Behavior of Scoliosis During Growth in Children with Osteogenesis Imperfecta av Alireza K. Anissipour, Kim Hammerberg, Angela Caudill, Т С Костюк, Sergey Tarima, Heather S. Zhao, Joseph J. Krzak, Peter A. Smith

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Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta av Walid El‐Sayed, David Parry, Richard F. Shore, Mushtaq Ahmed, Hussain Jafri, Yasmin Abdul Rashid, Suhaila Al‐Bahlani, Sharifa Al-Harasi, Jennifer Kirkham, Chris F. Inglehearn, Alan J. Mighell

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New perspectives on osteogenesis imperfecta av Antonella Forlino, Wayne A. Cabral, Aileen M. Barnes, Joan C. Marini

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Tooth dentin defects reflect genetic disorders affecting bone mineralization av Sibylle Vital, Céline Gaucher, Claire Bardet, Peter Rowe, Anne George, Agnès Linglart, Catherine Chaussain

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Phenotypic Variation in Dentinogenesis Imperfecta/Dentin Dysplasia Linked to 4q21 av Marsha Beattie, Jung‐Wook Kim, Siew‐Ging Gong, Carol Anne Murdoch‐Kinch, James P. Simmer, Jan C.‐C. Hu

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