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Reported noggin mutations are PCR errors.
Xu MQ, Shore EM, Kaplan FS. Xu MQ, et al. Am J Med Genet. 2002 Apr 22;109(2):161; author reply 163-4. doi: 10.1002/ajmg.10288. Am J Med Genet. 2002. PMID: 11977168 No abstract available.
Progressive osseous heteroplasia in the face of a child.
Faust RA, Shore EM, Stevens CE, Xu M, Shah S, Phillips CD, Kaplan FS. Faust RA, et al. Among authors: xu m. Am J Med Genet A. 2003 Apr 1;118A(1):71-5. doi: 10.1002/ajmg.a.10170. Am J Med Genet A. 2003. PMID: 12605446
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho TJ, Choi IH, Connor JM, Delai P, Glaser DL, LeMerrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS. Shore EM, et al. Among authors: xu m. Nat Genet. 2006 May;38(5):525-7. doi: 10.1038/ng1783. Epub 2006 Apr 23. Nat Genet. 2006. PMID: 16642017
Hematopoietic stem-cell contribution to ectopic skeletogenesis.
Kaplan FS, Glaser DL, Shore EM, Pignolo RJ, Xu M, Zhang Y, Senitzer D, Forman SJ, Emerson SG. Kaplan FS, et al. Among authors: xu m. J Bone Joint Surg Am. 2007 Feb;89(2):347-57. doi: 10.2106/JBJS.F.00472. J Bone Joint Surg Am. 2007. PMID: 17272450
Early diagnosis of fibrodysplasia ossificans progressiva.
Kaplan FS, Xu M, Glaser DL, Collins F, Connor M, Kitterman J, Sillence D, Zackai E, Ravitsky V, Zasloff M, Ganguly A, Shore EM. Kaplan FS, et al. Among authors: xu m. Pediatrics. 2008 May;121(5):e1295-300. doi: 10.1542/peds.2007-1980. Pediatrics. 2008. PMID: 18450872 Free PMC article.
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