Table of contents

Original articles

• Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome (1 March, 1999)

  Laurent Villard, Marie-Claude Bonino, Fatima Abidi, Angela Ragusa, Jérôme Belougne, Anne-Marie Lossi, Laurie Seaver, Jean-Paul Bonnefont, Corrado Romano, Marco Fichera, Didier Lacombe, André Hanauer, Nicole Philip, Charles Schwartz, Michel Fontés
• Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3–Xp22.11 (1 March, 1999)

  Koji Muroya, Ei-ichi Kinoshita, Tsutomu Kamimaki, Nobutake Matsuo, Tohru Yorifugi, Tsutomu Ogata
• Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR₃₀₀₀ (∼5.4 Mb) interval on chromosome 6q

  (1 March, 1999)

  Rebecca J Gardner, Andrew J Mungall, Ian Dunham, John C K Barber, Julian P H Shield, I Karen Temple, David O Robinson
• A clinical study of type 1 neurofibromatosis in north west England (1 March, 1999)

  J M McGaughran, D I Harris, D Donnai, D Teare, R MacLeod, R Westerbeek, H Kingston, M Super, R Harris, D G R Evans
• An analysis of common isodisomic regions in five mUPD 16 probands (1 March, 1999)

  Sayeda N Abu-Amero, Zehra Ali, Khaled K Abu-Amero, Philip Stanier, Gudrun E Moore
• A genetic study of the human T gene and its exclusion as a major candidate gene for sacral agenesis with anorectal atresia (1 March, 1999)

  Charalambos Papapetrou, Felicity Drummond, William Reardon, Robin Winter, Lewis Spitz, Yvonne H Edwards
• Genetic analysis of the 3′ untranslated region of the tumour necrosis factor shows a highly conserved region in rheumatoid arthritis affected and unaffected subjects (1 March, 1999)

  F Waldron-Lynch, C Adams, F Shanahan, M G Molloy, F O’Gara
• Investigation of germline GFRα-1 mutations in Hirschsprung disease (1 March, 1999)

  Shirley M Myers, Remi Salomon, Antje Goessling, Anna Pelet, Charis Eng, Andreas von Deimling, Stanislas Lyonnet, Lois M Mulligan
• A Hirschsprung disease locus at 22q11? (1 March, 1999)

  W S Kerstjens-Frederikse, R M W Hofstra, A J van Essen, J H C Meijers, C H C M Buys
• The inheritance of migraine with aura estimated by means of structural equation modelling (1 March, 1999)

  Vibeke Ulrich, Morten Gervil, Kirsten O Kyvik, Jes Olesen, Michael B Russell
• Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis (1 March, 1999)

  C Férec, O Raguénès, R Salomon, C Roche, J P Bernard, M Guillot, I Quéré, C Faure, B Mercier, M P Audrézet, P J Guillausseau, C Dupont, A Munnich, J D Bignon, L Le Bodic