TABLE OF CONTENTS

Volume 14, Issue 7 (July 2006)

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News and Commentary

Evolutionary Genetics: Is brain evolution still continuing in modern humans? FREE

Rowena Stern and Christopher Geoffrey Woods

Eur J Hum Genet 14: 799-800; advance online publication, March 29, 2006; doi:10.1038/sj.ejhg.5201624

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Letters

Congenital bilateral absence of the vas deferens and recombination at CFTR  FREE

David Haig

Eur J Hum Genet 14: 801; advance online publication, April 26, 2006; doi:10.1038/sj.ejhg.5201622

Reply to Professor Haig FREE

Pier Franco Pignatti

Eur J Hum Genet 14: 801; advance online publication, April 26, 2006; doi:10.1038/sj.ejhg.5201621

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Articles

Scientific rationality, uncertainty and the governance of human genetics: an interview study with researchers at deCODE genetics FREE

Stefán Hjörleifsson and Edvin Schei

Eur J Hum Genet 14: 802-808; advance online publication, April 19, 2006; doi:10.1038/sj.ejhg.5201626

Localization of candidate regions for a novel gene for Kartagener syndrome FREE

Ilse Gutierrez-Roelens, Thierry Sluysmans, Mark Jorissen, Mustapha Amyere and Miikka Vikkula

Eur J Hum Genet 14: 809-815; advance online publication, April 26, 2006; doi:10.1038/sj.ejhg.5201631

Mosaicism for mitochondrial DNA polymorphic variants in placenta has implications for the feasibility of prenatal diagnosis in mtDNA diseases FREE

David R Marchington, Martin Scott-Brown, David H Barlow and Joanna Poulton

Eur J Hum Genet 14: 816-823; advance online publication, May 3, 2006; doi:10.1038/sj.ejhg.5201618

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features FREE

Anna L Gloyn, Catherine Diatloff-Zito, Emma L Edghill, Christine Bellanné-Chantelot, Sylvie Nivot, Régis Coutant, Sian Ellard, Andrew T Hattersley and Jean Jacques Robert

Eur J Hum Genet 14: 824-830; advance online publication, May 3, 2006; doi:10.1038/sj.ejhg.5201629

Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11 FREE

N Simon Thomas, Miranda Durkie, Gemma Potts, Richard Sandford, Berendine Van Zyl, Sheila Youings, Nicholas R Dennis and Patricia A Jacobs

Eur J Hum Genet 14: 831-837; advance online publication, April 12, 2006; doi:10.1038/sj.ejhg.5201617

Differences in methylation patterns in the methylation boundary region of IDS gene in hunter syndrome patients: implications for CpG hot spot mutations FREE

Shunji Tomatsu, Kazuko Sukegawa, Georgeta G Trandafirescu, Monica A Gutierrez, Tatsuo Nishioka, Seiji Yamaguchi, Tadao Orii, Roseline Froissart, Irene Maire, Amparo Chabas, Alan Cooper, Paola Di Natale, Andreas Gal, Akihiko Noguchi and William S Sly

Eur J Hum Genet 14: 838-845; advance online publication, April 12, 2006; doi:10.1038/sj.ejhg.5201615

Genistein-mediated inhibition of glycosaminoglycan synthesis as a basis for gene expression-targeted isoflavone therapy for mucopolysaccharidoses FREE

Ewa Piotrowska, Joanna Jakóbkiewicz-Banecka, Sylwia Baran acuteska, Anna Tylki-Szyman acuteska, Barbara Czartoryska, Alicja We ogongrzyn and Grzegorz We ogongrzyn

Eur J Hum Genet 14: 846-852; advance online publication, May 3, 2006; doi:10.1038/sj.ejhg.5201623

Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional features FREE

Laura Belvederesi, Francesca Bianchi, Cristian Loretelli, Daniela Gagliardini, Eva Galizia, Raffaella Bracci, Saverio Rosati, Italo Bearzi, Alessandra Viel, Riccardo Cellerino and Emilio Porfiri

Eur J Hum Genet 14: 853-859; advance online publication, May 17, 2006; doi:10.1038/sj.ejhg.5201628

The influence of the alpha-adducin G460W polymorphism and angiotensinogen M235T polymorphism on antihypertensive medication and blood pressure FREE

Hedi Schelleman, Olaf H Klungel, Jacqueline C M Witteman, Albert Hofman, Cornelia M van Duijn, Anthonius de Boer and Bruno H C H Stricker

Eur J Hum Genet 14: 860-866; advance online publication, May 17, 2006; doi:10.1038/sj.ejhg.5201632

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q FREE

Anemone Finck, Jos W M Van der Meer, Alejandro A Schäffer, Jessica Pfannstiel, Claire Fieschi, Alessandro Plebani, A David B Webster, Lennart Hammarström and Bodo Grimbacher

Eur J Hum Genet 14: 867-875; advance online publication, April 26, 2006; doi:10.1038/sj.ejhg.5201634

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Short Reports

Sequence variations in the 5' upstream regions of the FBN1 gene associated with Marfan syndrome FREE

Krishna Kumar Singh, Praphulla Chandra Shukla, Kathrin Rommel, Jörg Schmidtke and Mine Arslan-Kirchner

Eur J Hum Genet 14: 876-879; advance online publication, April 12, 2006; doi:10.1038/sj.ejhg.5201620

Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma FREE

Sanna K Ylisaukko-oja, Cezary Cybulski, Rainer Lehtonen, Maija Kiuru, Joanna Matyjasik, Anna Szymañska, Jolanta Szymañska-Pasternak, Lars Dyrskjot, Ralf Butzow, Torben F Orntoft, Virpi Launonen, Jan Lubiñski and Lauri A Aaltonen

Eur J Hum Genet 14: 880-883; advance online publication, April 26, 2006; doi:10.1038/sj.ejhg.5201630

Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia FREE

Pradeep C Vasudevan, Stephen R F Twigg, John B Mulliken, Jackie A Cook, Oliver W J Quarrell and Andrew O M Wilkie

Eur J Hum Genet 14: 884-887; advance online publication, April 26, 2006; doi:10.1038/sj.ejhg.5201633

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Book Review

Handy Book on Cancer Genetics Risk Assessment FREE

Ulf Kristoffersson

Eur J Hum Genet 14: 888; doi:10.1038/sj.ejhg.5201641

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