TABLE OF CONTENTS
Volume 13, Issue 8 (August 2005)
News and Commentaries
Bioinformatics: Computers or clinicians for complex disease risk assessment? FREE
Carolyn Hoppe
Eur J Hum Genet 13: 893-894; advance online publication, May 11, 2005; doi:10.1038/sj.ejhg.5201441
Genomics: The amazing complexity of the human transcriptome FREE
Martin C Frith, Michael Pheasant and John S Mattick
Eur J Hum Genet 13: 894-897; advance online publication, June 22, 2005; doi:10.1038/sj.ejhg.5201459
Letter
Typing without calling the allele: a strategy for inferring SNP haplotypes FREE
Tamar Barzuza, Jacques S Beckmann, Ron Shamir and Itsik Pe'er
Eur J Hum Genet 13: 898-901; advance online publication, May 18, 2005; doi:10.1038/sj.ejhg.5201440
Articles
The population history of the Croatian linguistic minority of Molise (southern Italy): a maternal view FREE
Carla Babalini, Cristina Martínez-Labarga, Helle-Viivi Tolk, Toomas Kivisild, Rita Giampaolo, Tiziana Tarsi, Irene Contini, Lovorka Bara
, Branka Janiijevi, Irena Martinovi Klari, Marijana Peri
i, Anita Sujold
i, Richard Villems, Gianfranco Biondi, Pavao Rudan and Olga Rickards
Eur J Hum Genet 13: 902-912; advance online publication, May 11, 2005; doi:10.1038/sj.ejhg.5201439
Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma FREE
Anne-Sophie Jannot, Roubila Meziani, Guylene Bertrand, Benedicte Gérard, Vincent Descamps, Alain Archimbaud, Catherine Picard, Laurence Ollivaud, Nicole Basset-Seguin, Delphine Kerob, Guy Lanternier, Celeste Lebbe, P Saiag, Beatrice Crickx, Françoise Clerget-Darpoux, Bernard Grandchamp, Nadem Soufir and Melan-Cohort
Eur J Hum Genet 13: 913-920; advance online publication, April 27, 2005; doi:10.1038/sj.ejhg.5201415
Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome FREE
Isabella Borg, Kristine Freude, Sabine Kübart, Kirsten Hoffmann, Corinna Menzel, Franco Laccone, Helen Firth, Malcolm A Ferguson-Smith, Niels Tommerup, Hans-Hilger Ropers, David Sargan and Vera M Kalscheuer
Eur J Hum Genet 13: 921-927; advance online publication, May 4, 2005; doi:10.1038/sj.ejhg.5201429
RAR-related orphan receptor A isoform 1 (RORa1) is disrupted by a balanced translocation t(4;15)(q22.3;q21.3) associated with severe obesity FREE
Joakim Klar, Bengt Åsling, Birgit Carlsson, Magnus Ulvsbäck, Anita Dellsén, Carina Ström, Magdalena Rhedin, Anders Forslund, Göran Annerén, Jonas F Ludvigsson and Niklas Dahl
Eur J Hum Genet 13: 928-934; advance online publication, May 11, 2005; doi:10.1038/sj.ejhg.5201433
Genotype–phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy FREE
Ernie M H F Bongers, Frans T Huysmans, Elena Levtchenko, Jacky W de Rooy, Johan G Blickman, Ronald J C Admiraal, Patrick L M Huygen, Johannes R M Cruysberg, Pauline A M P Toolens, Judith B Prins, Paul F M Krabbe, George F Borm, Jeroen Schoots, Hans van Bokhoven, Angela M F van Remortele, Lies H Hoefsloot, Albert van Kampen and Nine V A M Knoers
Eur J Hum Genet 13: 935-946; advance online publication, June 1, 2005; doi:10.1038/sj.ejhg.5201446
The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study FREE
Terry G J Derks, Marinus Duran, Hans R Waterham, Dirk-Jan Reijngoud, Leo P ten Kate and G Peter A Smit
Eur J Hum Genet 13: 947-952; advance online publication, May 4, 2005; doi:10.1038/sj.ejhg.5201428
Short tandem repeats haplotyping of the HLA region in preimplantation HLA matching FREE
Francesco Fiorentino, Semra Kahraman, Hüseyin Karadayi, Anil Biricik, Semra Sertyel, Güvenc Karlikaya, Yaman Saglam, Daniele Podini, Andrea Nuccitelli and Marina Baldi
Eur J Hum Genet 13: 953-958; advance online publication, May 11, 2005; doi:10.1038/sj.ejhg.5201435
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs FREE
Liborio Stuppia, Ivana Antonucci, Francesco Binni, Alessandra Brandi, Nicoletta Grifone, Alessia Colosimo, Mariella De Santo, Valentina Gatta, Gianfranco Gelli, Valentina Guida, Silvia Majore, Giuseppe Calabrese, Chiara Palka, Anna Ravani, Rosanna Rinaldi, Gian Mario Tiboni, Enzo Ballone, Anna Venturoli, Alessandra Ferlini, Isabella Torrente, Paola Grammatico, Elisa Calzolari and Bruno Dallapiccola
Eur J Hum Genet 13: 959-964; advance online publication, May 4, 2005; doi:10.1038/sj.ejhg.5201437
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes FREE
Anna-Kaisa Niemi and Kari Majamaa
Eur J Hum Genet 13: 965-969; advance online publication, May 11, 2005; doi:10.1038/sj.ejhg.5201438
Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation FREE
Mahmoud Reza Mansouri, Lena Marklund, Peter Gustavsson, Edward Davey, Birgit Carlsson, Catharina Larsson, Irene White, Karl-Henrik Gustavson and Niklas Dahl
Eur J Hum Genet 13: 970-977; advance online publication, May 25, 2005; doi:10.1038/sj.ejhg.5201445
Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I FREE
Patrick Frosk, Marc R Del Bigio, Klaus Wrogemann and Cheryl R Greenberg
Eur J Hum Genet 13: 978-982; advance online publication, May 11, 2005; doi:10.1038/sj.ejhg.5201436
Short Reports
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes FREE
Maria Wehner, Elisabeth Mangold, Marlies Sengteller, Nicolaus Friedrichs, Stefan Aretz, Waltraut Friedl, Peter Propping and Constanze Pagenstecher
Eur J Hum Genet 13: 983-986; advance online publication, May 4, 2005; doi:10.1038/sj.ejhg.5201421
High-throughput pedigree drawing FREE
Ville-Petteri Mäkinen, Maija Parkkonen, Maija Wessman, Per-Henrik Groop, Timo Kanninen and Kimmo Kaski
Eur J Hum Genet 13: 987-989; advance online publication, May 4, 2005; doi:10.1038/sj.ejhg.5201430
Book Reviews
The pick of the crop FREE
Andrew John Walley
Eur J Hum Genet 13: 990; doi:10.1038/sj.ejhg.5201424
A most welcome new edition in a fast advancing field FREE
Carla Jodice
Eur J Hum Genet 13: 990-991; doi:10.1038/sj.ejhg.5201432
