TABLE OF CONTENTS
Volume 11, Issue 11 (November 2003)
Articles
Power of QTL detection using association tests with family controls FREE
Jules Hernández-Sánchez, Chris S Haley and Peter M Visscher
Eur J Hum Genet 11: 819-827; doi:10.1038/sj.ejhg.5201042
Meta and pooled analysis of European coeliac disease data FREE
Marie-Claude Babron, Staffan Nilsson, Svetlana Adamovic, Åsa Torinsson Naluai, Jan Wahlström, Henry Ascher, Paul J Ciclitira, Ludvig M Sollid, Jukka Partanen, Luigi Greco and Françoise Clerget-Darpoux the European Genetics Cluster on Coeliac Disease
Eur J Hum Genet 11: 828-834; doi:10.1038/sj.ejhg.5201051
Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2 FREE
Joanna S Zeiger, Jacqueline B Hetmanski, Terri H Beaty, Craig A VanderKolk, Diego F Wyszynski, Joan E Bailey-Wilson, Rosa Ortiz de Luna, Claudia Perandones, Marie M Tolarova, Terezie Mosby, Ricardo Bennun, Mabel Segovia, Pavel Calda, Elizabeth W Pugh, Kim Doheny and Iain McIntosh
Eur J Hum Genet 11: 835-839; doi:10.1038/sj.ejhg.5201052
The deleted in colorectal carcinoma (DCC) gene 201 R 
G polymorphism: no evidence for genetic association with autoimmune disease FREE
Richard J Hall, Marilyn E Merriman, Rachel A Green, Valerie H Markham, Deborah J Smyth, Joanne M Heward, Claire E Jennings, Antony W Braithwaite, Tim Cundy, Brian A Darlow, Peter J Gow, Andrew A Harrison, John Highton, Penny J Hunt, Patrick Manning, Violetta Pokorny, Russell S Scott, Barry J Taylor, Jinny A Willis, Sue Yeoman, Lachy McLean, Stephen CL Gough, Simon H Pearce and Tony R Merriman
Eur J Hum Genet 11: 840-844; doi:10.1038/sj.ejhg.5201059
Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population FREE
Marian Beekman, Bastiaan T Heijmans, Nicholas G Martin, John B Whitfield, Nancy L Pedersen, Ulf DeFaire, Harold Snieder, Nico Lakenberg, H Eka D Suchiman, Peter de Knijff, Rune R Frants, Gert Jan B van Ommen, Cornelis Kluft, George P Vogler, Dorret I Boomsma and P Eline Slagboom
Eur J Hum Genet 11: 845-850; doi:10.1038/sj.ejhg.5201053
Is the novel SCKL3 at 14q23 the predominant Seckel locus? FREE
Mehmet Okyay K
lnç, Vasiliki Ninidu Ninis, Sibel Aylin U[gcaron ]ur, Beyhan Tüysüz, Mehmet Seven, Sevim Balc, Judith Goodship and Aslhan Tolun
Eur J Hum Genet 11: 851-857; doi:10.1038/sj.ejhg.5201057
Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes FREE
Seval Türkmen, Gabriele Gillessen-Kaesbach, Peter Meinecke, Beate Albrecht, Luitgard M Neumann, Volker Hesse, Sükrü Palanduz, Stefanie Balg, Frank Majewski, Sigrun Fuchs, Petra Zschieschang, Monika Greiwe, Kirsten Mennicke, Friedmar R Kreuz, Harald J Dehmel, Burkhard Rodeck, Jürgen Kunze, Sigrid Tinschert, Stefan Mundlos and Denise Horn
Eur J Hum Genet 11: 858-865; doi:10.1038/sj.ejhg.5201050
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia FREE
Laura Lammi, Katri Halonen, Sinikka Pirinen, Irma Thesleff, Sirpa Arte and Pekka Nieminen
Eur J Hum Genet 11: 866-871; doi:10.1038/sj.ejhg.5201060
Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice FREE
Maria do Carmo Costa, Paula Magalhães, Fátima Ferreirinha, Laura Guimarães, Cristina Januário, Isabel Gaspar, Leal Loureiro, José Vale, Carolina Garrett, Fernando Regateiro, Marina Magalhães, Alda Sousa, Patrícia Maciel and Jorge Sequeiros
Eur J Hum Genet 11: 872-878; doi:10.1038/sj.ejhg.5201055
Short Reports
Karyotyping of human synaptonemal complexes by cenM-FISH FREE
Maria Oliver-Bonet, Thomas Liehr, Angela Nietzel, Anita Heller, Heike Starke, Uwe Claussen, Montserrat Codina-Pascual, Aïda Pujol, Carlos Abad, Josep Egozcue, Joaquima Navarro and Jordi Benet
Eur J Hum Genet 11: 879-883; doi:10.1038/sj.ejhg.5201067
No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's disease FREE
Dirk J de Jong, Barbara Franke, Anton HJ Naber, Judith JHT Willemen, Angelien JGAM Heister, Han G Brunner, Carolien GF de Kovel and Frans A Hol
Eur J Hum Genet 11: 884-887; doi:10.1038/sj.ejhg.5201058
Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms FREE
Päivi J Laitinen, Heikki Swan and Kimmo Kontula
Eur J Hum Genet 11: 888-891; doi:10.1038/sj.ejhg.5201061
Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2 FREE
Sixto Garcia-Miñaur, Lampros A Mavrogiannis, Sahan V Rannan-Eliya, Michael A Hendry, William A Liston, Mary E M Porteous and Andrew O M Wilkie
Eur J Hum Genet 11: 892-895; doi:10.1038/sj.ejhg.5201062
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion FREE
Marco Crimi, Roberto Del Bo, Sara Galbiati, Monica Sciacco, Andreina Bordoni, Nereo Bresolin and Giacomo Pietro Comi
Eur J Hum Genet 11: 896-898; doi:10.1038/sj.ejhg.5201056
