Table of contents

Letters to JMG

• Alterations of the Birt-Hogg-Dubé gene (BHD) in sporadic colorectal tumours

  (1 July, 2003)

  K Kahnoski, S K Khoo, N T Nassif, J Chen, G P Lobo, E Segelov, B T Teh
• A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3 (1 July, 2003)

  R G Ruf, J Berkman, M T F Wolf, P Nurnberg, M Gattas, E-M Ruf, V Hyland, J Kromberg, I Glass, J Macmillan, E Otto, G Nurnberg, B Lucke, H C Hennies, F Hildebrandt
• Mitotic recombination mediated by the JJAZF1 (KIAA0160) gene causing somatic mosaicism and a new type of constitutional NF1 microdeletion in two children of a mosaic female with only few manifestations

  (1 July, 2003)

  E Petek, D E Jenne, J Smolle, B Binder, W Lasinger, C Windpassinger, K Wagner, P M Kroisel, H Kehrer-Sawatzki
• Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion (1 July, 2003)

  C Gagliardi, M C Bonaglia, A Selicorni, R Borgatti, R Giorda
• High frequency of T9 and CFTR mutations in children with idiopathic bronchiectasis

  (1 July, 2003)

  V N Ninis, M O Kýlýnç, M Kandemir, E Daðlý, A Tolun
• FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics (1 July, 2003)

  B B A de Vries, L-A Severijnen, A Jacobs, R Olmer, D J J Halley, B A Oostra, R Willemsen
• A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2 (1 July, 2003)

  G F Leal, E Roberts, E O Silva, S M R Costa, D J Hampshire, C G Woods
• Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum (1 July, 2003)

  A Mubaidin, E Roberts, D Hampshire, M Dehyyat, A Shurbaji, M Mubaidien, A Jamil, A Al-Din, A Kurdi, C G Woods
• Myhre syndrome: new reports, review, and differential diagnosis (1 July, 2003)

  L Burglen, D Héron, A Moerman, A Dieux-Coeslier, J-P Bourguignon, A Bachy, J-C Carel, V Cormier-Daire, S Manouvrier, A Verloes