Table of contents

Research Article

• Psychological aspects of von Recklinghausen neurofibromatosis (NF1) (1 December, 1995)

  S E Mouridsen, S A Sørensen
• X inactivation of the FMR1 fragile X mental retardation gene. (1 December, 1995)

  C U Kirchgessner, S T Warren, H F Willard
• Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes. (1 December, 1995)

  I Stec, W Kress, G Meng, B Müller, C R Müller, T Grimm
• Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas. (1 December, 1995)

  C Eng, P A Crossey, L M Mulligan, C S Healey, C Houghton, A Prowse, S L Chew, P L Dahia, J L O'Riordan, S P Toledo
• Detection of germline mutations in the von Hippel-Lindau disease gene by the primer specified restriction map modification method. (1 December, 1995)

  T Kishida, F Chen, M I Lerman, B Zbar
• An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53. (1 December, 1995)

  J M Varley, G McGown, M Thorncroft, K J Tricker, M D Teare, M F Santibanez-Koref, J Martin, J M Birch, D G Evans
• Ophthalmic genetics: a genealogical guide to sources in England and Wales. (1 December, 1995)

  M Jay
• No evidence of genetic heterogeneity in dominant optic atrophy. (1 December, 1995)

  D Bonneau, E Souied, S Gerber, J M Rozet, E D'Haens, H Journel, G Plessis, J Weissenbach, A Munnich, J Kaplan
• Cluster headache is an autosomal dominantly inherited disorder in some families: a complex segregation analysis. (1 December, 1995)

  M B Russell, P G Andersson, L L Thomsen, L Iselius
• Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting. (1 December, 1995)

  A Schinzel, I Lorda-Sanchez, F Binkert, N P Carter, C E Bebb, M A Ferguson-Smith, U Eiholzer, M Zachmann, W P Robinson
• Cytogenetic and molecular findings in patients with Turner's syndrome stigmata. (1 December, 1995)

  T Kuznetzova, A Baranov, N Schwed, T Ivaschenko, P Malet, M Giollant, G A Savitsky, V Baranov
• Further delineation of the partial proximal trisomy 10q syndrome. (1 December, 1995)

  C M Aalfs, J M Hoovers, M A Nieste-Otter, M M Mannens, R C Hennekam, N J Leschot
• The Irish cystic fibrosis database. (1 December, 1995)

  S M Cashman, A Patino, M G Delgado, L Byrne, B Denham, M De Arce
• Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland. (1 December, 1995)

  P Guldberg, K F Henriksen, I Sipilä, F Güttler, A de la Chapelle
• Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria. (1 December, 1995)

  G Lundin, J Hashemi, Y Floderus, S Thunell, E Sagen, A Laegreid, W Wassif, T Peters, M Anvret
• A large multisite cancer family is linked to BRCA2. (1 December, 1995)

  P Tonin, P Ghadirian, C Phelan, G M Lenoir, H T Lynch, F Letendre, D Belanger, M Monté, S A Narod
• Familial café au lait spots: a variant of neurofibromatosis type 1. (1 December, 1995)

  D Abeliovich, Z Gelman-Kohan, S Silverstein, I Lerer, J Chemke, S Merin, J Zlotogora
• Partial disomy of Xp and the presence of SRY in a phenotypic female. (1 December, 1995)

  S Bajalica, E Blennow, A Tşezou, A Galla-Voumvouraki, M Alevizaki, C Sinaniotis, S Kitsiou-Tzeli
• Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques. (1 December, 1995)

  M B Qumsiyeh, A Tomasi, M Taslimi
• Del(3) (p25.3) without phenotypic effect. (1 December, 1995)

  L A Knight, M H Yong, M Tan, I S Ng
• Leukaemia and Sellafield: is there a heritable link? (1 December, 1995)

  G M Taylor, E J Tawn
• Severe intrauterine growth retardation with increased mitomycin C sensitivity, or Nijmegen breakage syndrome? (1 December, 1995)

  V M Der Kaloustian, A M Elliott, P Eydoux