Table of contents

Letters to JMG

• Association between markers in chromosomal region 17q23 and young onset hypertension: a TDT study (1 January, 2002)

  S-Y Wu, C S J Fann, Y-S Jou, J-W Chen, W-H Pan
• Paternal contribution to the risk for pre-eclampsia (1 January, 2002)

  P L M Zusterzeel, R te Morsche, M T M Raijmakers, E M Roes, W H M Peters, E A P Steegers
• Association of polymorphisms and allelic combinations in the tumour necrosis factor-α-complement MHC region with coronary artery disease (1 January, 2002)

  C Szalai, G Füst, J Duba, J Kramer, L Romics, Z Prohászka, A Császár
• CTLA-4/CD28 gene region is associated with genetic susceptibility to coeliac disease in UK families

  (1 January, 2002)

  A L King, S J Moodie, J S Fraser, D Curtis, E Reid, A M Dearlove, H J Ellis, P J Ciclitira
• A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cysts (1 January, 2002)

  Y Shinar, B Ben-Zeev, N Brand, H Lahat, V Gross-Zur, D MacGregor, T Bahan, D L Kastner, E Pras
• A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA (1 January, 2002)

  S Saviozzi, A Saluto, A M R Taylor, J I L Last, F Trebini, M C Paradiso, E Grosso, A Funaro, G Ponzio, N Migone, A Brusco
• In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patients (1 January, 2002)

  C Grayson, J P Chapple, K R Willison, A R Webster, A J Hardcastle, M E Cheetham
• Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new families

  (1 January, 2002)

  K Becker, PL Beales, D M Calver, G Matthijs, S N Mohammed
• Branchio-oculo-facial syndrome and branchio-otic/branchio-oto-renal syndromes are distinct entities (1 January, 2002)

  T Trummer, D Müller, A Schulze, W Vogel, W Just
• Infantile spinal muscular atrophy variant with congenital fractures in a female neonate: evidence for autosomal recessive inheritance (1 January, 2002)

  W Courtens, A-B Johansson, B Dachy, F Avni, N Telerman-Toppet, H Scheffer