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Proto-oncogene mutations in human breast cancer (HBC)

✍ Scribed by A. Ezzat; A. Abdul El-Warith; M.A. Ali; A.M. Abdulkareem; M. Senoussi; T. Amin; C.N. Adra


Book ID
119157436
Publisher
Elsevier Science
Year
1991
Weight
179 KB
Volume
27
Category
Article
ISSN
0277-5379

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Human piebaldism: six novel mutations of
✍ Petros Syrris; Kirsten Heathcote; Romeo Carrozzo; Koen Devriendt; Nursel ElΓ§iogl πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 127 KB

Human piebaldism is a rare autosomal dominant disorder that comprises congenital patchy depigmentation of the scalp, forehead, trunk and limbs. It is caused by mutations in the cell-surface receptor tyrosine kinase gene (KIT, also c-kit). We screened three families and three isolated cases of piebal