Drugs: endocrine system

The oestrogen receptor α gene is linked and/or associated with age of menarche in different ethnic groups
J-R Long, H Xu, L-J Zhao, P-Y Liu, H Shen, Y-J Liu, D-H Xiong, P Xiao, Y-Z Liu, V Dvornyk, J-L Li, R R Recker, H-W Deng

Journal of Medical Genetics Oct 2005, 42 (10) 796-800; DOI: 10.1136/jmg.2004.028381
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
G McGillivray, R Savarirayan, T C Cox, C Stojkoski, R McNeil, A Bankier, J F Bateman, T Roscioli, R J M Gardner, S R Lamandé

Journal of Medical Genetics Aug 2005, 42 (8) 656-662; DOI: 10.1136/jmg.2004.027888
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1
HG Kim, S R Herrick, E Lemyre, S Kishikawa, J A Salisz, S Seminara, M E MacDonald, G A P Bruns, C C Morton, B J Quade, J F Gusella

Journal of Medical Genetics Aug 2005, 42 (8) 666-672; DOI: 10.1136/jmg.2004.026989
A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5
S G Cole, M E Begbie, G M F Wallace, C L Shovlin

Journal of Medical Genetics Jul 2005, 42 (7) 577-582; DOI: 10.1136/jmg.2004.028712
Interleukin 12 gene polymorphisms enhance gastric cancer risk in H pylori infected individuals
F Navaglia, D Basso, C-F Zambon, E Ponzano, L Caenazzo, N Gallo, A Falda, C Belluco, P Fogar, E Greco, F Di Mario, M Rugge, M Plebani

Journal of Medical Genetics Jun 2005, 42 (6) 503-510; DOI: 10.1136/jmg.2004.022723
Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study
D Lambrechts, K Devriendt, D A Driscoll, E Goldmuntz, M Gewillig, R Vlietinck, D Collen, P Carmeliet

Journal of Medical Genetics Jun 2005, 42 (6) 519-522; DOI: 10.1136/jmg.2004.026443
TNFα and IL10 SNPs act together to predict disease behaviour in Crohn’s disease
E V Fowler, R Eri, G Hume, S Johnstone, N Pandeya, D Lincoln, D Templeton, G L Radford-Smith

Journal of Medical Genetics Jun 2005, 42 (6) 523-528; DOI: 10.1136/jmg.2004.027425
VEGF polymorphisms and severity of atherosclerosis
W M Howell, S Ali, M J Rose-Zerilli, S Ye

Journal of Medical Genetics Jun 2005, 42 (6) 485-490; DOI: 10.1136/jmg.2004.025734
STK11 genotyping and cancer risk in Peutz-Jeghers syndrome
V Schumacher, T Vogel, B Leube, C Driemel, T Goecke, G Möslein, B Royer-Pokora

Journal of Medical Genetics May 2005, 42 (5) 428-435; DOI: 10.1136/jmg.2004.026294
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts
A M Sharp, L M Messiaen, G Page, C Antignac, M-C Gubler, L F Onuchic, S Somlo, G G Germino, L M Guay-Woodford

Journal of Medical Genetics Apr 2005, 42 (4) 336-349; DOI: 10.1136/jmg.2004.024489

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