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Saudi Medical Journal|June 11, 2020
Molecular and clinical characteristics of very-long-chain acyl-CoA dehydrogenase deficiency: A single-center experience in Saudi ArabiaAmal Alhashem, Sarar Mohamed, Manal Abdelraheem, et al.Human Mutation|November 20, 2010
Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collectionGeorge P Patrinos, Jumana Al Aama, Aida Al Aqeel, et al.Human Molecular Genetics|April 3, 2007
Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growthRebecca A Mosig, Oonagh Dowling, Analisa DiFeo, 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 1