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pro vyhledávání: '"Meena A"'
Publikováno v:
Familial Cancer. 6:463-471
Neurofibromatosis type 1 is a common familial cancer syndrome, affecting about 1 in every 4,000 individuals worldwide. We have carried out NF1 gene mutation analysis on DNA isolated from 25 tumours (dermal and plexiform neurofibromas, malignant perip
Autor:
J. P. Traynor, S. Griffiths, N. F. Őnen, A. Cooke, Edward S. Tobias, William Stewart, Meena Upadhyaya, M. Balsitis, A. A. Shah
Publikováno v:
Familial Cancer. 6:147-152
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominantly inherited conditions. A range of complications has been described, including gastrointestinal manifestations. Gastric carcinoid tumours are associated with multiple endocri
Publikováno v:
Familial cancer. 6(1)
Our experience of providing an NF1 gene diagnostic mutation detection service as part of the U.K. Genetic Testing Network (UKGTN) is presented. A total of 169 unrelated individuals suspected of having neurofibromatosis type I (NF1) were referred for
Publikováno v:
Familial Cancer; Mar2007, Vol. 6 Issue 1, p21-34, 14p