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WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.
Laine CM, Joeng KS, Campeau PM, Kiviranta R, Tarkkonen K, Grover M, Lu JT, Pekkinen M, Wessman M, Heino TJ, Nieminen-Pihala V, Aronen M, Laine T, Kröger H, Cole WG, Lehesjoki AE, Nevarez L, Krakow D, Curry CJ, Cohn DH, Gibbs RA, Lee BH, Mäkitie O. Laine CM, et al. Among authors: laine t. N Engl J Med. 2013 May 9;368(19):1809-16. doi: 10.1056/NEJMoa1215458. N Engl J Med. 2013. PMID: 23656646 Free PMC article.
A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis.
Laine CM, Wessman M, Toiviainen-Salo S, Kaunisto MA, Mäyränpää MK, Laine T, Pekkinen M, Kröger H, Välimäki VV, Välimäki MJ, Lehesjoki AE, Mäkitie O. Laine CM, et al. Among authors: laine t. J Bone Miner Res. 2015 Mar;30(3):510-8. doi: 10.1002/jbmr.2355. J Bone Miner Res. 2015. PMID: 25209159 Free article.
Diagnosis of Osteoporosis in Children and Adolescents.
Laine CM, Laine T. Laine CM, et al. Among authors: laine t. Eur Endocrinol. 2013 Aug;9(2):141-144. doi: 10.17925/EE.2013.09.02.141. Epub 2013 Aug 23. Eur Endocrinol. 2013. PMID: 29922371 Free PMC article. Review.
174 results