TABLE OF CONTENTS
Volume 13, Issue 4 (April 2005)
News and Commentaries
Cancer Genetics: Activated Notch takes center stage in T-cell leukemogenesis FREE
Mark Y Chiang and Warren S Pear
Eur J Hum Genet 13: 393-395; advance online publication, February 9, 2005; doi:10.1038/sj.ejhg.5201380
Research Network: EUROGLYCANET: a European network focused on congenital disorders of glycosylation FREE
Gert Matthijs
Eur J Hum Genet 13: 395-397; advance online publication, December 22, 2004; doi:10.1038/sj.ejhg.5201359
Cascade Screening: Whose information is it anyway? FREE
Guido de Wert
Eur J Hum Genet 13: 397-398; advance online publication, January 26, 2005; doi:10.1038/sj.ejhg.5201373
Letters
Confidentiality and serious harm in genetics FREE
Angus Clarke
Eur J Hum Genet 13: 399; advance online publication, January 12, 2005; doi:10.1038/sj.ejhg.5201349
Dilemma still not resolved FREE
Anneke Lucassen and Michael Parker
Eur J Hum Genet 13: 399-400; advance online publication, January 12, 2005; doi:10.1038/sj.ejhg.5201350
Articles
Cascade testing in familial hypercholesterolaemia: how should family members be contacted? FREE
Ainsley J Newson and Steve E Humphries
Eur J Hum Genet 13: 401-408; advance online publication, January 19, 2005; doi:10.1038/sj.ejhg.5201360
Combination of WAGR and Potocki–Shaffer contiguous deletion syndromes in a patient with an 11p11.2–p14 deletion FREE
Dominique Brémond-Gignac, John A Crolla, Henri Copin, Agnès Guichet, Dominique Bonneau, Laurence Taine, Didier Lacombe, Clarisse Baumann, Brigitte Benzacken and Alain Verloes
Eur J Hum Genet 13: 409-413; advance online publication, January 26, 2005; doi:10.1038/sj.ejhg.5201358
Defective protein glycosylation in patients with cutis laxa syndrome FREE
Eva Morava, Suzan Wopereis, Paul Coucke, Gabrielle Gillessen-Kaesbach, Thomas Voit, Jan Smeitink, Ron Wevers and Stephanie Grünewald
Eur J Hum Genet 13: 414-421; advance online publication, January 19, 2005; doi:10.1038/sj.ejhg.5201361
Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients FREE
Jian Yu Xu, Qing Hong Dan, Vivian Chan, Nelson M S Wat, Sidney Tam, Sau Cheung Tiu, Ka Fai Lee, Shing Chung Siu, Man Wo Tsang, Lai Ming Fung, Kin Wah Chan and Karen S L Lam
Eur J Hum Genet 13: 422-427; advance online publication, December 15, 2004; doi:10.1038/sj.ejhg.5201347
Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations FREE
Marta Ribasés, Mònica Gratacòs, Fernando Fernández-Aranda, Laura Bellodi, Claudette Boni, Marija Anderluh, Maria Cristina Cavallini, Elena Cellini, Daniela Di Bella, Stefano Erzegovesi, Christine Foulon, Mojca Gabrovsek, Philip Gorwood, Johannes Hebebrand, Anke Hinney, Jo Holliday, Xun Hu, Andreas Karwautz, Amélie Kipman, Radovan Komel, Benedetta Nacmias, Helmut Remschmidt, Valdo Ricca, Sandro Sorbi, Martina Tomori, Gudrun Wagner, Janet Treasure, David A Collier and Xavier Estivill
Eur J Hum Genet 13: 428-434; advance online publication, December 22, 2004; doi:10.1038/sj.ejhg.5201351
Sequence variation in the ATP8B1 gene and intrahepatic cholestasis of pregnancy FREE
Jodie N Painter, Miia Savander, Anne Ropponen, Nina Nupponen, Seija Riikonen, Olavi Ylikorkala, Anna-Elina Lehesjoki and Kristiina Aittomäki
Eur J Hum Genet 13: 435-439; advance online publication, January 12, 2005; doi:10.1038/sj.ejhg.5201355
A common CTLA4 haplotype associated with coeliac disease FREE
Karen A Hunt, Dermot P B McGovern, Parveen J Kumar, Subrata Ghosh, Simon P L Travis, Julian R F Walters, Derek P Jewell, Raymond J Playford and David A van Heel
Eur J Hum Genet 13: 440-444; advance online publication, January 12, 2005; doi:10.1038/sj.ejhg.5201357
Polymorphisms in APOA1 and LPL genes are statistically independently associated with fasting TG in men with CAD FREE
Olga W Souverein, J Wouter Jukema, S Matthijs Boekholdt, Aeilko H Zwinderman and Michael W T Tanck
Eur J Hum Genet 13: 445-451; advance online publication, January 19, 2005; doi:10.1038/sj.ejhg.5201362
X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations FREE
Maris Laan, Victor Wiebe, Elza Khusnutdinova, Maido Remm and Svante Pääbo
Eur J Hum Genet 13: 452-462; advance online publication, December 22, 2004; doi:10.1038/sj.ejhg.5201340
Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations FREE
Gittan Kollberg, Monica Jansson, Åsa Pérez-Bercoff, Atle Melberg, Christopher Lindberg, Elisabeth Holme, Ali-Reza Moslemi and Anders Oldfors
Eur J Hum Genet 13: 463-469; advance online publication, February 9, 2005; doi:10.1038/sj.ejhg.5201341
Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations FREE
Geraldine R Vink, Stefan J White, Strelicija Gabelic, Pancras C W Hogendoorn, Martijn H Breuning and Egbert Bakker
Eur J Hum Genet 13: 470-474; advance online publication, December 8, 2004; doi:10.1038/sj.ejhg.5201343
Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR FREE
Qingfa Wu, Erik Niebuhr, Huanming Yang and Lars Hansen
Eur J Hum Genet 13: 475-485; advance online publication, January 19, 2005; doi:10.1038/sj.ejhg.5201345
Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes FREE
Osman El-Maarri, Muhieddine Seoud, Jean-Baptiste Rivière, Johannes Oldenburg, Jörn Walter, Guy Rouleau and Rima Slim
Eur J Hum Genet 13: 486-490; advance online publication, January 12, 2005; doi:10.1038/sj.ejhg.5201353
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia FREE
Cecilia Marino, Roberto Giorda, Maria Luisa Lorusso, Laura Vanzin, Nello Salandi, Maria Nobile, Alessandra Citterio, Silvana Beri, Valentina Crespi, Marco Battaglia and Massimo Molteni
Eur J Hum Genet 13: 491-499; advance online publication, January 26, 2005; doi:10.1038/sj.ejhg.5201356
Short Reports
Uroplakin III is not a major candidate gene for primary vesicoureteral reflux FREE
Helena Kelly, Sean Ennis, Akihiro Yoneda, Claire Bermingham, Denis C Shields, Cliona Molony, Andrew J Green, Prem Puri and David E Barton
Eur J Hum Genet 13: 500-502; advance online publication, November 3, 2004; doi:10.1038/sj.ejhg.5201322
A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome FREE
Thomy J L de Ravel, Indira B Taylor, Alex J T Van Oostveldt, Jean-Pierre Fryns and Andrew O M Wilkie
Eur J Hum Genet 13: 503-505; advance online publication, November 3, 2004; doi:10.1038/sj.ejhg.5201325
No germline FH mutations in familial breast cancer patients FREE
Maija Kiuru, Rainer Lehtonen, Hannaleena Eerola, Kristiina Aittomäki, Carl Blomqvist, Heli Nevanlinna, Lauri A Aaltonen and Virpi Launonen
Eur J Hum Genet 13: 506-509; advance online publication, November 3, 2004; doi:10.1038/sj.ejhg.5201326
Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation FREE
Florian Hoffmann, Peter Lohse, Silvia Stojanov, Yoon S Shin, Ellen D Renner, Anja Kéry, Stephanie Zellerer and Bernd H Belohradsky
Eur J Hum Genet 13: 510-512; advance online publication, December 22, 2004; doi:10.1038/sj.ejhg.5201352
Unexpected high frequency of P46L TNFRSF1A allele in sub-Saharan West African populations FREE
Dimitri Tchernitchko, Mihelaiti Chiminqgi, Frédéric Galactéros, Claude Préhu, Yvon Segbena, Hamidou Coulibaly, Nadia Rebaya and Sylvain Loric
Eur J Hum Genet 13: 513-515; advance online publication, December 8, 2004; doi:10.1038/sj.ejhg.5201344
