Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia by ROBINS, Tiina, BELLANNE-CHANTELOT, Christine, BARBARO, Michela, CABROL, Sylvie, WEDELL, Anna, LAJIC, Svetlana

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Molecular Model of Human CYP21 Based on Mammalian CYP2C5: Structural Features Correlate with Clinical Severity of Mutations Causing Congenital Adrenal Hyperplasia by Robins, Tiina, Carlsson, Jonas, Sunnerhagen, Maria, Wedell, Anna, Persson, Bengt

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Not All Amino Acid Substitutions of the Common Cluster E6 Mutation in CYP21 Cause Congenital Adrenal Hyperplasia by Robins, Tiina, Barbaro, Michela, Lajic, Svetlana, Wedell, Anna

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Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran by Baradaran-Heravi, Alireza, Vakili, Rahim, Robins, Tiina, Carlsson, Jonas, Ghaemi, Nosrat, A'rabi, Azadeh, Abbaszadegan, Mohammad Reza

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Molecular Model of Human CYP21 Based onMammalian CYP2C5: Structural Features Correlatewith Clinical Severity of Mutations CausingCongenital Adrenal Hyperplasia by Robins, Tiina, Carlsson, Jonas, Sunnerhagen, Maria, Wedell, Anna, Persson, Bengt

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Novel mutations in CYP21 detected in individuals with hyperandrogenism by LAJIC, Svetlana, CLAUIN, Séverine, ROBINS, Tiina, VEXIAU, Patrick, BLANCHE, Hélène, BELIANNE-CHANTELOT, Christine, WEDELL, Anna

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CYP21 mutations in simple virilizing congenital adrenal hyperplasia by LAJIC, Svetlana, ROBINS, Tiina, KRONE, Nils, SCHWARZ, Hans P, WEDELL, Anna

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Novel Mutations in CYP21 Detected in Individuals with Hyperandrogenism by Lajić, Svetlana, Clauin, Séverine, Robins, Tiina, Vexiau, Patrick, Blanché, Hélène, Bellanne-Chantelot, Christine, Wedell, Anna

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Early human occupation of Australia’s eastern seaboard by Adams, Shaun, Norman, Kasih, Kemp, Justine, Jacobs, Zenobia, Costelloe, Michael, Fairbairn, Andrew, Robins, Richard, Stock, Errol, Moss, Patrick, Smith, Tam, Love, Serena, Manne, Tiina, Lowe, Kelsey M., Logan, India, Manoel, Michael, McFadden, Karen, Burns, Darren, Dooley, Thomas, Falkiner, Zac, Clarkson, Chris

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Author Correction: Early human occupation of Australia’s eastern seaboard by Adams, Shaun, Norman, Kasih, Kemp, Justine, Jacobs, Zenobia, Costelloe, Michael, Fairbairn, Andrew, Robins, Richard, Stock, Errol, Moss, Patrick, Smith, Tam, Love, Serena, Manne, Tiina, Lowe, Kelsey M., Logan, India, Manoel, Michael, McFadden, Karen, Burns, Darren, Dooley, Thomas, Falkiner, Zac, Clarkson, Chris

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Overview of hereditary breast and ovarian cancer (HBOC) guidelines across Europe by Marmolejo, David Humberto, Wong, Mark Yu Zheng, Bajalica-Lagercrantz, Svetlana, Tischkowitz, Marc, Balmaña, Judith, Patócs, Attila Balázs, Chappuis, Pierre, Colas, Chrystelle, Genuardi, Maurizio, Haanpää, Maria, Vetti, Hildegunn Hoberg, Hoogerbrugge, Nicoline, Irmejs, Arvids, Kahre, Tiina, Klink, Barbara, Krajc, Mateja, Milagre, Tamara Hussong, de Putter, Robin, Steinke-Lange, Verena, Wadt, Karin, Wimmer, Katharina

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A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation by BRAMON, Elvira, PIRINEN, Matti, LANGFORD, Cordelia, DELOUKAS, Panos, HUNT, Sarah, GRAY, Emma, DRONOV, Serge, POTTER, Simon C, TASHAKKORI-GHANBARIA, Avazeh, EDKINS, Sarah, BUMPSTEAD, Suzannah J, ARRANZ, Maria J, STRANGE, Amy, BAKKER, Steven, BENDER, Stephan, BRUGGEMAN, Richard, CAHN, Wiepke, CHANDLER, David, COLLIER, David A, CRESPO-FACORRO, Benedicto, DAZZAN, Paola, DE HAAN, Lieuwe, DI FORTI, Marta, KUANG LIN, DRAGOVIC, Milan, GIEGLING, Ina, HALL, Jeremy, LYEGBE, Conrad, JOBLENSKY, Assen, KAHN, René S, KALAYDJIEVA, Luba, KRAVARITI, Eugenia, LAWRIE, Stephen, LINSZEN, Don H, FREEMAN, Colin, MATA, Ignacio, MCDONALD, Colm, MCINTOSH, Andrew, MYIN-GERMEYS, Inez, OPHOFF, Roel A, PARIANTE, Carmine M, PAUNIO, Tiina, PICCHIONI, Marco, RIPKE, Stephan, RUJESCU, Dan, BELLENGUEZ, Celine, SAUER, Heinrich, SHAIKH, Madiha, SUSSMANN, Jessika, SUVISAARI, Jaana, TOSATO, Sarah, TOULOPOULOU, Timothea, VAN OS, Jim, WALSHE, Muriel, WEISBROD, Matthias, WHALLEY, Heather, ZHAN SU, BAND, Gavin, PEARSON, Richard, VUKCEVIC, Damjan

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