TABLE OF CONTENTS
Volume 15, Issue 4 (April 2007)
Practical Genetics
CHARGE syndrome: an update FREE
Damien Sanlaville and Alain Verloes
Eur J Hum Genet 15: 389-399; advance online publication, February 14, 2007; doi:10.1038/sj.ejhg.5201778
Letters
'Distorted' mitochondrial DNA sequences in schizophrenic patients FREE
Hans-Jürgen Bandelt, Anna Olivieri, Claudio Bravi, Yong-Gang Yao, Antonio Torroni and Antonio Salas
Eur J Hum Genet 15: 400-402; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201781
Reply to Bandelt et al FREE
Lourdes Martorell and Elisabet Vilella
Eur J Hum Genet 15: 402-404; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201782
Articles
FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias FREE
Ana Beleza-Meireles, Fredrik Lundberg, Kristina Lagerstedt, Xiaolei Zhou, Davood Omrani, Louise Frisén and Agneta Nordenskjöld
Eur J Hum Genet 15: 405-410; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201777
Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature FREE
Siulan Vendramini, Antonio Richieri-Costa and Maria Leine Guion-Almeida
Eur J Hum Genet 15: 411-421; advance online publication, February 7, 2007; doi:10.1038/sj.ejhg.5201770
Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism FREE
Dries Castermans, Joris R Vermeesch, Jean-Pierre Fryns, Jean G Steyaert, Wim J M Van de Ven, John W M Creemers and Koen Devriendt
Eur J Hum Genet 15: 422-431; advance online publication, February 7, 2007; doi:10.1038/sj.ejhg.5201785
Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations FREE
Cécile Mignon-Ravix, Danielle Depetris, Judith J Luciani, Cristina Cuoco, Malgorzata Krajewska-Walasek, Chantal Missirian, Patrick Collignon, Bruno Delobel, Marie-Françoise Croquette, Anne Moncla, Peter M Kroisel and Marie-Geneviève Mattei
Eur J Hum Genet 15: 432-440; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201775
Distribution of the D15Z1 copy number polymorphism FREE
Annette E Cockwell, Patricia A Jacobs and John A Crolla
Eur J Hum Genet 15: 441-445; advance online publication, February 21, 2007; doi:10.1038/sj.ejhg.5201780
Genotype–phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française' FREE
Mylène Béri-Deixheimer, Marie-José Gregoire, Annick Toutain, Karène Brochet, Sylvain Briault, Jean-Luc Schaff, Bruno Leheup and Philippe Jonveaux
Eur J Hum Genet 15: 446-452; advance online publication, February 7, 2007; doi:10.1038/sj.ejhg.5201784
The complexity of reproductive decision-making in asymptomatic carriers of the Huntington mutation FREE
Marleen Decruyenaere, Gerry Evers-Kiebooms, Andrea Boogaerts, Kristien Philippe, Koen Demyttenaere, René Dom, Wim Vandenberghe and Jean-Pierre Fryns
Eur J Hum Genet 15: 453-462; advance online publication, January 24, 2007; doi:10.1038/sj.ejhg.5201774
Linkage and association analysis of CACNG3 in childhood absence epilepsy FREE
Kate V Everett, Barry Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer, Petra Callenbach, Athanasios Covanis, Olivier Dulac, Orvar Eeg-Olofsson, Martha Feucht, Mogens Friis, Françoise Goutieres, Renzo Guerrini, Armin Heils, Marianne Kjeldsen, Anna-Elina Lehesjoki, Andrew Makoff, Rima Nabbout, Ingrid Olsson, Thomas Sander, Auli Sirén, Paul McKeigue, Robert Robinson, Nichole Taske, Michele Rees and Mark Gardiner
Eur J Hum Genet 15: 463-472; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201783
A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation FREE
Catherine Dehainault, Dorothée Michaux, Sabine Pagès-Berhouet, Virginie Caux-Moncoutier, François Doz, Laurence Desjardins, Jérôme Couturier, Philippe Parent, Dominique Stoppa-Lyonnet, Marion Gauthier-Villars and Claude Houdayer
Eur J Hum Genet 15: 473-477; advance online publication, February 14, 2007; doi:10.1038/sj.ejhg.5201787
Angiotensinogen M235T polymorphism and the risk of myocardial infarction and stroke among hypertensive patients on ACE-inhibitors or 
-blockers FREE
Hedi Schelleman, Olaf H Klungel, Jacqueline C M Witteman, Monique M B Breteler, Moygan Yazdanpanah, A H Jan Danser, Albert Hofman, Cornelia M van Duijn, Anthonius de Boer and Bruno H Ch Stricker
Eur J Hum Genet 15: 478-484; advance online publication, February 14, 2007; doi:10.1038/sj.ejhg.5201789
Paleolithic Y-haplogroup heritage predominates in a Cretan highland plateau FREE
Laisel Martinez, Peter A Underhill, Lev A Zhivotovsky, Tenzin Gayden, Nicholas K Moschonas, Cheryl-Emiliane T Chow, Simon Conti, Elisabetta Mamolini, L Luca Cavalli-Sforza and Rene J Herrera
Eur J Hum Genet 15: 485-493; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201769
Short Reports
Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample FREE
Katja Kivinen, Hanna Peterson, Leena Hiltunen, Hannele Laivuori, Sanna Heino, Inkeri Tiala, Sakari Knuutila, Vesa Rasi and Juha Kere
Eur J Hum Genet 15: 494-497; advance online publication, February 7, 2007; doi:10.1038/sj.ejhg.5201788
Ashkenazi Jewish mtDNA haplogroup distribution varies among distinct subpopulations: lessons of population substructure in a closed group FREE
Jeanette Feder, Ofer Ovadia, Benjamin Glaser and Dan Mishmar
Eur J Hum Genet 15: 498-500; advance online publication, January 24, 2007; doi:10.1038/sj.ejhg.5201764
Most pooling variation in array-based DNA pooling is attributable to array error rather than pool construction error FREE
Stuart Macgregor
Eur J Hum Genet 15: 501-504; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201768
Large genomic rearrangements in NIPBL are infrequent in Cornelia de Lange Syndrome FREE
Zahurul A Bhuiyan, Helen Stewart, Egbert J Redeker, Marcel M A M Mannens and Raoul C M Hennekam
Eur J Hum Genet 15: 505-508; advance online publication, January 31, 2007; doi:10.1038/sj.ejhg.5201776
