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Genetic Factors in Canine Narcolepsy 由 Arthur S. Foutz, Merrill M. Mitler, Luigi Luca Cavalli-Sforza, William C. Dement

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Hereditary myeloperoxidase deficiency 由 M Kitahara, H.J. Eyre, Y Simonian, CL Atkin, SJ Hasstedt

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A founder mutation of the potassium channel KCNQ1 in long QT syndrome 由 Kirsi Piippo, Heikki Swan, Michael Pasternack, Hugh Chapman, Kristian Paavonen, Matti Viitasalo, Lauri Toivonen, Kimmo Kontula

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Low Prevalence of Risk Markers in Cases of Sudden Death Due to Brugada Syndrome 由 Hariharan Raju, Michael Papadakis, Malini Govindan, Rachel Bastiaenen, Navin Chandra, Ann L. O’Sullivan, Georgina Baines, Sanjay Sharma, Elijah R. Behr

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Family Studies in Narcolepsy 由 Michel Billiard, V. Pasquié-Magnetto, Michael G. Heckman, Bertrand Carlander, A Besset, Zachari I Zachariev, J.-F. Eliaou, Alain Malafosse

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Deficiency of plasma plasminogen activator inhibitor 1 results in hyperfibrinolytic bleeding 由 M. H. Lee, Evan Vosburgh, K. C. Anderson, J McDonagh

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Anxiety disorders in fragile X premutation carriers: Preliminary characterization of probands and non-probands 由 Lisa Cordeiro, Floridette Abucayan, Randi J. Hagerman, Flora Tassone, David Hessl

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Prevalence of <i>BRCA1</i> and <i>BRCA2</i> mutations in Ashkenazi Jewish families with breast and pancreatic cancer 由 Zsofia K. Stadler, Erin Salo‐Mullen, Sujata M. Patil, M. Catherine Pietanza, Joseph Vijai, Emmanouil Saloustros, Nichole Hansen, Noah D. Kauff, Robert C. Kurtz, David P. Kelsen, Kenneth Offit, Mark E. Robson

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STAG3 truncating variant as the cause of primary ovarian insufficiency 由 Polona Le Quesne Stabej, Hywel Williams, Chela James, Mehmet Tekman, Horia Stanescu, Robert Kleta, Louise Ocaka, Francesco Lescai, Helen L. Storr, Maria Bitner‐Glindzicz, Chiara Bacchelli, Gerard S. Conway

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Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil 由 Juliana Giacomazzi, Simone Geiger de Almeida Selistre, Cristina Rossi, Bárbara Alemar, Patrícia Santos-Silva, Fernando Schell Pereira, Cristina Netto, Silvia Liliana Cossio, Daniela Elaine Roth, Algemir Lunardi Brunetto, Marcelo Zagonel de Oliveira, Ghyslaine Martel‐Planche, José Roberto Goldim, Pierre Hainaut, Suzi Alves Camey, Patrícia Ashton‐Prolla

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A Novel <i>IFITM5</i> Mutation in Severe Atypical Osteogenesis Imperfecta Type VI Impairs Osteoblast Production of Pigment Epithelium-Derived Factor 由 Charles R. Farber, Adi Reich, Aileen M. Barnes, Patricia Becerra, Frank Rauch, Wayne A. Cabral, Alison Bae, Aaron R. Quinlan, Francis H. Glorieux, Thomas L. Clemens, Joan C. Marini

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Expression of hemochromatosis in homozygous subjects 由 Lawrie W. Powell, Kim Summers, Phillip G. Board, E. Axelsen, Sonja Webb, June W. Halliday

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Mitochondrial myopathy and myoclonic epilepsy 由 Walter O. Arruda, Luíz Fernando Bleggi Torres, Anne Lombès, Salvatore DiMauro, Belkiss A. Cardoso, Hélio Afonso Ghizoni Teive, Duilton de Paola, Ricardo R. Seixas

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Association study of T102C 5-HT_2A polymorphism in schizophrenic patients: diagnosis, psychopathology, and suicidal behavior 由 Humberto Corrêa, Luiz De Marco, Wolfanga L. Boson, Rodrigo Nicolato, Antó L. Teixeira, Valdir R. Campo, Marco Aurélio Romano‐Silva

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Familial breast cancer in southern Finland 由 Hannaleena Eerola, Carl Blomqvist, ­Eero Pukkala, Seppo Pyrhönen, Heli Nevanlinna

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Synthesis of a shortened pro-alpha 2(I) chain and decreased synthesis of pro-alpha 2(I) chains in a proband with osteogenesis imperfecta. 由 W J de Wet, Taina Pihlajaniemi, Jeanne C. Myers, Thaddeus E. Kelly, Darwin J. Prockop

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Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency 由 Todor Arsov, Saul A. Mullen, John A. Damiano, Kate Lawrence, Linda Huh, Melinda Nolan, Helen Young, Anaïs Thouin, Hans‐Henrik M. Dahl, Samuel F. Berkovic, Douglas E. Crompton, Lynette G. Sadleir, Ingrid E. Scheffer

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Substance use disorders in adolescents with attention deficit hyperactivity disorder: a 4-year follow-up study 由 Annabeth P. Groenman, Jaap Oosterlaan, Nanda Rommelse, Barbara Franke, Herbert Roeyers, Robert D. Oades, Joseph A. Sergeant, Jan K. Buitelaar, Stephen V. Faraone

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Whole‐genome copy number variation analysis in anophthalmia and microphthalmia 由 KF Schilter, Linda M. Reis, Adele Schneider, TM Bardakjian, Omar Abdul‐Rahman, BA Kozel, HH Zimmerman, Ulrich Broeckel, EV Semina

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Presence of c.3956delC mutation in familial adenomatous polyposis patients from Brazil 由 Caroline Aquino Moreira-Nunes, Diego Di Felipe Ávila Alcântara, Sérgio Figueiredo Lima-Júnior, Sandro Roberto de Araújo Cavalléro, Juan A. Rey, Giovanny R. Pinto, Paulo Pimentel de Assumpção, Rommel Mário Rodríguez Burbano

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