Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome represent one condition with variable expression and age‐related penetrance: results of a clinical study of PTEN mutation carriers
AUTOR(ES)
Lachlan, K L
FONTE
BMJ Group
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2597943Documentos Relacionados
- Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
- Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes*
- Síndrome de Bannayan-Riley-Ruvalcaba com hamartomas lipomatosos deformantes em lactente - Relato de caso
- Age-related macular disease.
- Age-related factors in carcinogenesis
