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Familial Cancer|November 15, 2024
The genetic landscape of Lynch syndrome in the Israeli populationAasem Abu Shtaya, Sofia Naftaly Nathan, Inbal Kedar, et al.Human Molecular Genetics|September 6, 2012
Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagenUlrike Schwarze, Tim Cundy, Shawna M Pyott, et al.Pageof 3