TABLE OF CONTENTS
Volume 15, Issue 8 (August 2007)
News and Commentary
Vascular Pathologies: Angiogenomics: towards a genetic nosology and understanding of vascular anomalies FREE
Miikka Vikkula
Eur J Hum Genet 15: 821-822; advance online publication, May 16, 2007; doi:10.1038/sj.ejhg.5201856
Articles
Specific combinations of HLA-DR2 and DR3 class II haplotypes contribute graded risk for disease susceptibility and autoantibodies in human SLE FREE
Robert R Graham, Ward Ortmann, Peter Rodine, Karl Espe, Carl Langefeld, Ethan Lange, Adrienne Williams, Stephanie Beck, Chieko Kyogoku, Kathy Moser, Patrick Gaffney, Peter K Gregersen, Lindsey A Criswell, John B Harley and Timothy W Behrens
Eur J Hum Genet 15: 823-830; advance online publication, April 4, 2007; doi:10.1038/sj.ejhg.5201827
Estimating cancer risk in HNPCC by the GRL method FREE
Flora Alarcon, Christine Lasset, Jérôme Carayol, Valérie Bonadona, Hervé Perdry, Françoise Desseigne, Qing Wang and Catherine Bonaïti-Pellié
Eur J Hum Genet 15: 831-836; advance online publication, May 2, 2007; doi:10.1038/sj.ejhg.5201843
Confirmation of EP300 gene mutations as a rare cause of Rubinstein–Taybi syndrome FREE
Nicole Zimmermann, Ana Maria Bravo Ferrer Acosta, Jürgen Kohlhase and Oliver Bartsch
Eur J Hum Genet 15: 837-842; advance online publication, February 14, 2007; doi:10.1038/sj.ejhg.5201791
Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients FREE
Marianne Stef, Delphine Simon, Béatrice Mardirossian, Marie-Ange Delrue, Ingrid Burgelin, Christophe Hubert, Michèle Marche, Françoise Bonnet, Philippe Gorry, Michel Longy, Didier Lacombe, Isabelle Coupry and Benoît Arveiler
Eur J Hum Genet 15: 843-847; advance online publication, May 2, 2007; doi:10.1038/sj.ejhg.5201847
Transcriptional regulation of TLX2 and impaired intestinal innervation: possible role of the PHOX2A and PHOX2B genes FREE
Silvia Borghini, Marco Di Duca, Giuseppe Santamaria, Manuela Vargiolu, Tiziana Bachetti, Francesca Cargnin, Alessio Pini Prato, Roberto De Giorgio, Margherita Lerone, Vincenzo Stanghellini, Vincenzo Jasonni, Diego Fornasari, Roberto Ravazzolo and Isabella Ceccherini
Eur J Hum Genet 15: 848-855; advance online publication, May 16, 2007; doi:10.1038/sj.ejhg.5201852
Differential haplotypic expression of the interleukin-18 gene FREE
Sandrine Barbaux, Odette Poirier, Tiphaine Godefroy, Hartmut Kleinert, Stefan Blankenberg, François Cambien and Laurence Tiret
Eur J Hum Genet 15: 856-863; advance online publication, May 9, 2007; doi:10.1038/sj.ejhg.5201842
Estimating the odds ratios of Crohn disease for the main CARD15/NOD2 mutations using a conditional maximum likelihood method in pedigrees collected via affected family members FREE
Leigh Pascoe, Habib Zouali, Mourad Sahbatou and Jean-Pierre Hugot
Eur J Hum Genet 15: 864-871; advance online publication, April 25, 2007; doi:10.1038/sj.ejhg.5201839
Genetic influences on angina pectoris and its impact on coronary heart disease FREE
Slobodan Zdravkovic, Andreas Wienke, Nancy L Pedersen and Ulf de Faire
Eur J Hum Genet 15: 872-877; advance online publication, May 9, 2007; doi:10.1038/sj.ejhg.5201846
Genotypic and haplotypic associations of the DBH gene with plasma dopamine 
-hydroxylase activity in African Americans FREE
Yi-lang Tang, Michael P Epstein, George M Anderson, Cyrus P Zabetian and Joseph F Cubells
Eur J Hum Genet 15: 878-883; advance online publication, April 25, 2007; doi:10.1038/sj.ejhg.5201838
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine FREE
Kaate R J Vanmolkot, Anine H Stam, Ashok Raman, Jan B Koenderink, Boukje de Vries, Eelke H van den Boogerd, Judith van Vark, Jeroen J M W van den Heuvel, Nin Bajaj, Gisela M Terwindt, Joost Haan, Rune R Frants, Michel D Ferrari and Arn M J M van den Maagdenberg
Eur J Hum Genet 15: 884-888; advance online publication, May 2, 2007; doi:10.1038/sj.ejhg.5201841
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23–q24 FREE
Alessia Deglincerti, Roberto De Giorgio, Kivanc Cefle, Marcella Devoto, Tommaso Pippucci, Giovanni Castegnaro, Emanuele Panza, Giovanni Barbara, Rosanna F Cogliandro, Zeynel Mungan, Sukru Palanduz, Roberto Corinaldesi, Giovanni Romeo, Marco Seri and Vincenzo Stanghellini
Eur J Hum Genet 15: 889-897; advance online publication, May 9, 2007; doi:10.1038/sj.ejhg.5201844
Short Reports
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia FREE
R Alex Henderson, Kathy Williamson, Sally Cumming, Michael P Clarke, Sally Ann Lynch, Isabel M Hanson, David R FitzPatrick, Sanjay Sisodiya and Veronica van Heyningen
Eur J Hum Genet 15: 898-901; advance online publication, April 4, 2007; doi:10.1038/sj.ejhg.5201826
An explanation for another familial case of Rett syndrome: maternal germline mosaicism FREE
Margarida Venâncio, Mónica Santos, Susana Aires Pereira, Patrícia Maciel and Jorge M Saraiva
Eur J Hum Genet 15: 902-904; advance online publication, April 18, 2007; doi:10.1038/sj.ejhg.5201835
Book Reviews
So that is why you stink! FREE
Patrick Macleod
Eur J Hum Genet 15: 905-906; doi:10.1038/sj.ejhg.5201857
Molecular Bases of Mental Retardation FREE
Cristina Rusu
Eur J Hum Genet 15: 906-907; doi:10.1038/sj.ejhg.5201861
En route towards genetic medicine in practice: a clinical genetics guide in the post genomic era FREE
Stanislas Lyonnet
Eur J Hum Genet 15: 907; doi:10.1038/sj.ejhg.5201864
Corrigendum
Association study of major risk single nucleotide polymorphisms in the common regulatory region of PARK2 and PACRG genes with leprosy in an Indian population FREE
Dheeraj Malhotra, Katayoon Darvishi, Manmohan Lohra, Himanshu Kumar, Chander Grover, Soni Sood, Belum S N Reddy and Ramesh N K Bamezai
Eur J Hum Genet 15: 908; doi:10.1038/sj.ejhg.5201903
