Table of contents

Original articles

• Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome (19 September, 2008)

  M J Lyons, J M Graham, G Neri, A G W Hunter, R D Clark, R C Rogers, M Moscarda, L Boccuto, R Simensen, J Dodd, S Robertson, B R DuPont, M J Friez, C E Schwartz, R E Stevenson
• Mutation in the HPGD gene encoding NAD⁺ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC)

  (19 September, 2008)

  M Tariq, Z Azeem, G Ali, M S Chishti, W Ahmad
• Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background (9 September, 2008)

  C Krausz, C Giachini, Y Xue, M K O’Bryan, J Gromoll, E Rajpert-de Meyts, R Oliva, I Aknin-Seifer, E Erdei, N Jorgensen, M Simoni, J L Ballescà, R Levy, G Balercia, P Piomboni, E Nieschlag, G Forti, R McLachlan, C Tyler-Smith
• Functional polymorphisms in the BRCA1 promoter influence transcription and are associated with decreased risk for breast cancer in Chinese women

  (9 September, 2008)

  K Y-K Chan, W Liu, J-R Long, S-P Yip, S-Y Chan, X-O Shu, D T-T Chua, A N-Y Cheung, J C-Y Ching, H Cai, G K-H Au, M Chan, W Foo, H Y-S Ngan, Y-T Gao, E S-W Ngan, M-M Garcia-Barceló, Wei Zheng, U-S Khoo
• Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy (19 September, 2008)

  D Araújo-Vilar, G Lattanzi, B González-Méndez, A T Costa-Freitas, D Prieto, M Columbaro, E Mattioli, B Victoria, N Martínez-Sánchez, A Ramazanova, M Fraga, A Beiras, J Forteza, L Domínguez-Gerpe, C Calvo, J Lado-Abeal