TABLE OF CONTENTS
Volume 14, Issue 5 (May 2006)
Editorial
Assisted reproduction and genetics FREE
Helena Kääriäinen
Eur J Hum Genet 14: 505; doi:10.1038/sj.ejhg.5201609
News and Commentary
Human Genome: Which proteins contribute to human-chimpanzee differences? FREE
Justin Fay
Eur J Hum Genet 14: 506; advance online publication, March 8, 2006; doi:10.1038/sj.ejhg.5201596
Williams–Beuren Syndrome: More or less? Segmental duplications and deletions in the Williams–Beuren syndrome region provide new insights into language development FREE
May Tassabehji and Dian Donnai
Eur J Hum Genet 14: 507-508; advance online publication, March 8, 2006; doi:10.1038/sj.ejhg.5201597
Policy
The need for interaction between assisted reproduction technology and genetics FREE
Eur J Hum Genet 14: 509-511; doi:10.1038/sj.ejhg.5201600
Review
Schizophrenia genetics: uncovering positional candidate genes FREE
Maria Karayiorgou and Joseph A Gogos
Eur J Hum Genet 14: 512-519; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201587
Articles
New variants in the mitochondrial genomes of schizophrenic patients FREE
Lourdes Martorell, Teresa Segués, Gerard Folch, Joaquín Valero, Jorge Joven, Antonio Labad and Elisabet Vilella
Eur J Hum Genet 14: 520-528; advance online publication, March 15, 2006; doi:10.1038/sj.ejhg.5201606
Use of phenotypic covariates in association analysis by sequential addition of cases FREE
Stuart Macgregor, Nick Craddock and Peter A Holmans
Eur J Hum Genet 14: 529-534; advance online publication, March 15, 2006; doi:10.1038/sj.ejhg.5201604
A text-mining analysis of the human phenome FREE
Marc A van Driel, Jorn Bruggeman, Gert Vriend, Han G Brunner and Jack A M Leunissen
Eur J Hum Genet 14: 535-542; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201585
MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34 FREE
Daniel J Hampshire, Mohammed Ayub, Kelly Springell, Emma Roberts, Hussain Jafri, Yasmin Rashid, Jacquelyn Bond, John H Riley and C Geoffrey Woods
Eur J Hum Genet 14: 543-548; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201577
Postzygotic mutation and germline mosaicism in the otopalatodigital syndrome spectrum disorders FREE
Stephen P Robertson, Sarah Thompson, Timothy Morgan, Muriel Holder-Espinasse, Véronique Martinot-Duquenoy, Andrew O M Wilkie and Sylvie Manouvrier-Hanu
Eur J Hum Genet 14: 549-554; advance online publication, March 15, 2006; doi:10.1038/sj.ejhg.5201586
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine FREE
Kaate R J Vanmolkot, Esther E Kors, Ulku Turk, Dylsad Turkdogan, Antoine Keyser, Ludo A M Broos, Sima Kheradmand Kia, Jeroen J M W van den Heuvel, David F Black, Joost Haan, Rune R Frants, Virginia Barone, Michel D Ferrari, Giorgio Casari, Jan B Koenderink and Arn M J M van den Maagdenberg
Eur J Hum Genet 14: 555-560; advance online publication, March 15, 2006; doi:10.1038/sj.ejhg.5201607
Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor FREE
Jens Plaschke, Michael Linnebacher, Matthias Kloor, Johannes Gebert, Friedrich W Cremer, Sigrid Tinschert, Daniela E Aust, Magnus von Knebel Doeberitz and Hans K Schackert
Eur J Hum Genet 14: 561-566; advance online publication, January 18, 2006; doi:10.1038/sj.ejhg.5201568
Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms FREE
Claude Férec, Teresa Casals, Nadia Chuzhanova, Milan Macek Jr, Thierry Bienvenu, Andrea Holubova, Caitriona King, Trudi McDevitt, Carlo Castellani, Philip M Farrell, Molly Sheridan, Sarah-Jane Pantaleo, Ourida Loumi, Taieb Messaoud, Harry Cuppens, Francesca Torricelli, Garry R Cutting, Robert Williamson, Maria Jesus Alonso Ramos, Pier Franco Pignatti, Odile Raguénès, David N Cooper, Marie-Pierre Audrézet and Jian-Min Chen
Eur J Hum Genet 14: 567-576; advance online publication, February 22, 2006; doi:10.1038/sj.ejhg.5201590
Y-chromosomal STR haplotype analysis reveals surname-associated strata in the East-German population FREE
Uta-Dorothee Immel, Michael Krawczak, Jürgen Udolph, Angela Richter, Heike Rodig, Manfred Kleiber and Michael Klintschar
Eur J Hum Genet 14: 577-582; advance online publication, January 25, 2006; doi:10.1038/sj.ejhg.5201572
Short Report
A novel mutation in JARID1C gene associated with mental retardation FREE
Cristina Santos, Laia Rodriguez-Revenga, Irene Madrigal, Celia Badenas, Merce Pineda and Montserrat Milà
Eur J Hum Genet 14: 583-586; advance online publication, March 15, 2006; doi:10.1038/sj.ejhg.5201608
Book Review
Clinical genetics: Medical genetics FREE
Claude Stoll
Eur J Hum Genet 14: 587; doi:10.1038/sj.ejhg.5201601
Policy
The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues FREE
Sirpa Soini, Dolores Ibarreta, Violetta Anastasiadou, Ségolène Aymé, Suzanne Braga, Martina Cornel, Domenico A Coviello, Gerry Evers-Kiebooms, Joep Geraedts, Luca Gianaroli, Joyce Harper, György Kosztolanyi, Kersti Lundin, Emilio Rodrigues-Cerezo, Karen Sermon, Jorge Sequeiros, Lisbeth Tranebjaerg and Helena Kääriäinen on behalf of ESHG and ESHRE
Eur J Hum Genet 14: 588-645; doi:10.1038/sj.ejhg.5201598
