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Other Oncology
Citations 1-10 of 91 total displayed.
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Most recent content
(1 Apr 2006):
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- Electronic letters
Influence of glutathione-S-transferase (GSTM1, GSTP1, GSTT1) and cytochrome p450 (CYP1A1, CYP2D6) polymorphisms on numbers of basal cell carcinomas (BCCs) in families with the naevoid basal cell carcinoma syndrome
- X (R) Yang, R M Pfeiffer, and A M Goldstein
J Med Genet 2006; 43: e16.
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Past content
(since Jan 1999):
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- Letters to JMG
Penetrance of adrenocortical tumours associated with the germline TP53 R337H mutation
- B C Figueiredo, R Sandrini, G P Zambetti, R M Pereira, C Cheng, W Liu, L Lacerda, M A Pianovski, E Michalkiewicz, J Jenkins, C Rodriguez-Galindo, M J Mastellaro, S Vianna, F Watanabe, F Sandrini, S B I Arram, P Boffetta, and R C Ribeiro
J Med Genet 2006 43: 91 -96; published online before print as 10.1136/jmg.2004.030551
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- Original articles
Alternative mechanisms associated with silencing of CDKN1C in Beckwith–Wiedemann syndrome
- N Diaz-Meyer, Y Yang, S N Sait, E R Maher, and M J Higgins
J Med Genet 2005; 42: 648-655.
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- Original articles
STRA13 expression and subcellular localisation in normal and tumour tissues: implications for use as a diagnostic and differentiation marker
- A Ivanova, S-Y Liao, M I Lerman, S Ivanov, and E J Stanbridge
J Med Genet 2005; 42: 565-576.
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- Original articles
Classification of BRCA1 missense variants of unknown clinical significance
- C M Phelan, V Dapic, B Tice, R Favis, E Kwan, F Barany, S Manoukian, P Radice, R B van der Luijt, B P M van Nesselrooij, G Chenevix-Trench, kConFab, T Caldes, M de La Hoya, S Lindquist, S V Tavtigian, D Goldgar, Å Borg, S A Narod, and A N A Monteiro
J Med Genet 2005; 42: 138-146.
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[ Erratum ]
- Letters to JMG
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour
- S Reid, A Renwick, S Seal, L Baskcomb, R Barfoot, H Jayatilake, The Breast Cancer Susceptibility Collaboration (UK), K Pritchard-Jones, M R Stratton, A Ridolfi-Lüthy, N Rahman for the Familial Wilms Tumour Collaboration
J Med Genet 2005; 42: 147-151.
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- Reviews
Referral for cancer genetics consultation: a review and compilation of risk assessment criteria
- H Hampel, K Sweet, J A Westman, K Offit, and C Eng
J Med Genet 2004; 41: 81-91.
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- Electronic letters
Comorbid VHL and SCA2 mutations in a large kindred: confounding diagnosis of neurological dysfunction caused by CNS VHL vascular tumours versus SCA2 atrophic neurodegeneration
- D E McNeil, W M Linehan, and G M Glenn
J Med Genet 2002; 39: e37.
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- Letters to the editor
Oncology nurse training in cancer genetics
- Clara Gaff, Kristiina Aittomäki, and Robert Williamson
J Med Genet 2001; 38: 691-695.
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- Letters to the editor
A distinct splice form of APC is highly expressed in neurones but not commonly mutated in neuroepithelial tumours
- KIRA STEIGERWALD, IRMA M SANTORO, JENNIFER J KORDICH, VIVIANA GISMONDI, CHRIS TRZEPACZ, MANUELA BADIALI, F GIANGASPERO, M GREGORY BALKO, JENNIFER S GRAHAM, NANCY RATNER, ANDREW M LOWY, LILIANA VARESCO, and JOANNA GRODEN
J Med Genet 2001; 38: 257-262.
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