TABLE OF CONTENTS
Volume 15, Issue 11 (November 2007)
News and Commentary
Deletions Revealing Recessive Genes: Deletions that reveal recessive genes FREE
David J Coman and RJ McKinlay Gardner
Eur J Hum Genet 15: 1103-1104; advance online publication, August 29, 2007; doi:10.1038/sj.ejhg.5201919
Policy
Guidelines for molecular karyotyping in constitutional genetic diagnosis
Joris Robert Vermeesch, Heike Fiegler, Nicole de Leeuw, Karoly Szuhai, Jacqueline Schoumans, Roberto Ciccone, Frank Speleman, Anita Rauch, Jill Clayton-Smith, Conny Van Ravenswaaij, Damien Sanlaville, Philippos C Patsalis, Helen Firth, Koen Devriendt and Orsetta Zuffardi
Eur J Hum Genet 15: 1105-1114; advance online publication, July 18, 2007; doi:10.1038/sj.ejhg.5201896
Articles
A new mutation in TP63 is associated with age-related pathology
Muriel Holder-Espinasse, Dominique Martin-Coignard, Fabienne Escande and Sylvie Manouvrier-Hanu
Eur J Hum Genet 15: 1115-1120; advance online publication, July 4, 2007; doi:10.1038/sj.ejhg.5201888
Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses
Kirsten Marie Sanggaard, Nanna Dahl Rendtorff, Klaus Wilbrandt Kjaer, Hans Eiberg, Torsten Johnsen, Steen Gimsing, Jørgen Dyrmose, Kristian Otto Nielsen, Kasper Lage and Lisbeth Tranebjærg
Eur J Hum Genet 15: 1121-1131; advance online publication, July 18, 2007; doi:10.1038/sj.ejhg.5201900
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf–Hirschhorn syndrome
Klara Flipsen-ten Berg, Peter M van Hasselt, Marc J Eleveld, Suzanne E van der Wijst, Frans A Hol, Monique A M de Vroede, Frits A Beemer, P F Ron Hochstenbach and Martin Poot
Eur J Hum Genet 15: 1132-1138; advance online publication, July 18, 2007; doi:10.1038/sj.ejhg.5201899
Risk estimation for familial breast cancer: improving the system of counselling
Helen Gregory, Sarah Wordsworth, Barbara Gibbons, Brenda Wilson and Neva Haites
Eur J Hum Genet 15: 1139-1144; advance online publication, July 18, 2007; doi:10.1038/sj.ejhg.5201895
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
Marianne Lévêque, Sandrine Marlin, Laurence Jonard, Vincent Procaccio, Pascal Reynier, Patrizia Amati-Bonneau, Sylvain Baulande, Denis Pierron, Didier Lacombe, Françoise Duriez, Christine Francannet, Thierry Mom, Hubert Journel, Hélène Catros, Valérie Drouin-Garraud, Marie-Françoise Obstoy, Hélène Dollfus, Marie-Madeleine Eliot, Laurence Faivre, Christian Duvillard, Remy Couderc, Eréa-Noël Garabedian, Christine Petit, Delphine Feldmann and Françoise Denoyelle
Eur J Hum Genet 15: 1145-1155; advance online publication, July 18, 2007; doi:10.1038/sj.ejhg.5201891
The efficiency of nonsense-mediated mRNA decay is an inherent character and varies among different cells
Liat Linde, Stephanie Boelz, Gabriele Neu-Yilik, Andreas E Kulozik and Batsheva Kerem
Eur J Hum Genet 15: 1156-1162; advance online publication, July 11, 2007; doi:10.1038/sj.ejhg.5201889
Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease
Susan Winkler, Inke R König, Katja Lohmann-Hedrich, Peter Vieregge, Vladimir Kostic and Christine Klein
Eur J Hum Genet 15: 1163-1168; advance online publication, July 18, 2007; doi:10.1038/sj.ejhg.5201901
Two-stage association tests for genome-wide association studies based on family data with arbitrary family structure
Tao Feng, Shuanglin Zhang and Qiuying Sha
Eur J Hum Genet 15: 1169-1175; advance online publication, July 25, 2007; doi:10.1038/sj.ejhg.5201902
Genetic analysis of the GRM1 gene in human melanoma susceptibility
Pablo Ortiz, Francisco Vanaclocha, Eduardo López-Bran, José Ignacio Esquivias, José Luis López-Estebaranz, Manuel Martín-González, Itziar Arrue, Diana García-Romero, Carolina Ochoa, Antonio González-Perez, Agustin Ruiz and Luis Miguel Real
Eur J Hum Genet 15: 1176-1182; advance online publication, July 4, 2007; doi:10.1038/sj.ejhg.5201887
Short Reports
Co-introgression of Y-chromosome haplogroups and the sickle cell gene across Africa's Sahel
Rihab E Bereir, Hisham Y Hassan, Niven A Salih, Peter A Underhill, Luigi L Cavalli-Sforza, Ayman A Hussain, Dominic Kwiatkowski and Muntaser E Ibrahim
Eur J Hum Genet 15: 1183-1185; advance online publication, August 15, 2007; doi:10.1038/sj.ejhg.5201892
A functional mutation in the LDLR promoter (-139C>G) in a patient with familial hypercholesterolemia
Andrew JP Smith, Fayha Ahmed, Devi Nair, Ros Whittall, Darrell Wang, Alison Taylor, Gail Norbury and Steve E Humphries
Eur J Hum Genet 15: 1186-1189; advance online publication, July 11, 2007; doi:10.1038/sj.ejhg.5201897
Book Review
Consent and confidentiality: Consent and Confidentiality in Genetic Practice
Domenico Coviello
Eur J Hum Genet 15: 1190; doi:10.1038/sj.ejhg.5201898
