Table of contents

Letters to JMG

• Assignment of a new congenital fibrosis of extraocular muscles type 3 (CFEOM3) locus, FEOM4, based on a balanced translocation t(2;13) (q37.3;q12.11) and identification of candidate genes

  (2 March, 2005)

  P Aubourg, M Krahn, R Bernard, K Nguyen, O Forzano, I Boccaccio, V Delague, A De Sandre-Giovannoli, J Pouget, D Depétris, M-G Mattei, N Philip, N Lévy
• Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11 (2 March, 2005)

  A De Sandre-Giovannoli, V Delague, T Hamadouche, M Chaouch, M Krahn, I Boccaccio, T Maisonobe, E Chouery, R Jabbour, S Atweh, D Grid, A Mégarbané, N Lévy
• Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study (2 March, 2005)

  H Qu, M-C Tessier, T J Hudson, C Polychronakos
• MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta (2 March, 2005)

  J-W Kim, J P Simmer, T C Hart, P S Hart, M D Ramaswami, J D Bartlett, J C-C Hu
• Complete allelic analysis of BRCA1 and BRCA2 variants in young Nigerian breast cancer patients

  (2 March, 2005)

  J D Fackenthal, L Sveen, Q Gao, E K Kohlmeir, C Adebamowo, T O Ogundiran, A A Adenipekun, R Oyesegun, O Campbell, C Rotimi, E E U Akang, S Das, O I Olopade
• Prevalence and phenotype of subjects carrying rare variants in the Italian registry for alpha₁-antitrypsin deficiency

  (2 March, 2005)

  I Ferrarotti, J Baccheschi, M Zorzetto, C Tinelli, L Corda, B Balbi, I Campo, E Pozzi, G Faa, P Coni, G Massi, G Stella, M Luisetti