Journal of Medical Genetics: 42 (9)

Electronic letters

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)
(1 September, 2005)
M Nielsen, P F Franken, T H C M Reinards, M M Weiss, A Wagner, H van der Klift, S Kloosterman, J J Houwing-Duistermaat, C M Aalfs, M G E M Ausems, A H J T Bröcker-Vriends, E B Gomez Garcia, N Hoogerbrugge, F H Menko, R H Sijmons, S Verhoef, E J Kuipers, H Morreau, M H Breuning, C M J Tops, J T Wijnen, H F A Vasen, R Fodde, F J Hes
Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma
(1 September, 2005)
D P Dimasi, A W Hewitt, C M Green, D A Mackey, J E Craig
Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification
(1 September, 2005)
J Douglas, K Tatton-Brown, K Coleman, S Guerrero, J Berg, T R P Cole, D FitzPatrick, Y Gillerot, H E Hughes, D Pilz, F L Raymond, I K Temple, A Irrthum, J P Schouten, N Rahman

Collagen VI related muscle disorders (1 September, 2005)
A K Lampe, K M D Bushby

Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes (1 September, 2005)
G Piluso, L Politano, S Aurino, M Fanin, E Ricci, V M Ventriglia, A Belsito, A Totaro, V Saccone, H Topaloglu, A C Nascimbeni, L Fulizio, A Broccolini, N Canki-Klain, L I Comi, G Nigro, C Angelini, V Nigro
The MDM2 promoter polymorphism SNP309T→G and the risk of uterine leiomyosarcoma, colorectal cancer, and squamous cell carcinoma of the head and neck
(1 September, 2005)
P Alhopuro, S K Ylisaukko-oja, W J Koskinen, P Bono, J Arola, H J Järvinen, J-P Mecklin, T Atula, R Kontio, A A Mäkitie, S Suominen, I Leivo, P Vahteristo, L-M Aaltonen, L A Aaltonen

Cancer risks in BRCA2 families: estimates for sites other than breast and ovary
(1 September, 2005)
C J van Asperen, R M Brohet, E J Meijers-Heijboer, N Hoogerbrugge, S Verhoef, H F A Vasen, M G E M Ausems, F H Menko, E B Gomez Garcia, J G M Klijn, F B L Hogervorst, J C van Houwelingen, L J van’t Veer, M A Rookus, F E van Leeuwen
Association of genes of lipid metabolism with measures of subclinical cardiovascular disease in the Diabetes Heart Study (1 September, 2005)
K P Burdon, C D Langefeld, S R Beck, L E Wagenknecht, J J Carr, B I Freedman, D Herrington, D W Bowden
ASPM mutations identified in patients with primary microcephaly and seizures
(1 September, 2005)
J Shen, W Eyaid, G H Mochida, F Al-Moayyad, A Bodell, C G Woods, C A Walsh
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1 (1 September, 2005)
A Slavotinek, S S Lee, R Davis, A Shrit, K A Leppig, J Rhim, K Jasnosz, D Albertson, D Pinkel