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Severe hypodontia and oral xanthomas in Alagille syndrome.
Ho NC, Lacbawan F, Francomano CA, Ho V. Ho NC, et al. Among authors: ho v. Am J Med Genet. 2000 Jul 31;93(3):250-2. doi: 10.1002/1096-8628(20000731)93:3<250::aid-ajmg18>3.0.co;2-a. Am J Med Genet. 2000. PMID: 10925392 No abstract available.
Comprehensive resource: Skeletal gene database.
Jia L, Ho NC, Park SS, Powell J, Francomano CA. Jia L, et al. Among authors: ho nc. Am J Med Genet. 2001 Winter;106(4):275-81. doi: 10.1002/ajmg.10227. Am J Med Genet. 2001. PMID: 11891679
A skeletal gene database.
Ho NC, Jia L, Driscoll CC, Gutter EM, Francomano CA. Ho NC, et al. J Bone Miner Res. 2000 Nov;15(11):2095-122. doi: 10.1359/jbmr.2000.15.11.2095. J Bone Miner Res. 2000. PMID: 11092392 Free article.
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia.
Arikawa-Hirasawa E, Le AH, Nishino I, Nonaka I, Ho NC, Francomano CA, Govindraj P, Hassell JR, Devaney JM, Spranger J, Stevenson RE, Iannaccone S, Dalakas MC, Yamada Y. Arikawa-Hirasawa E, et al. Among authors: ho nc. Am J Hum Genet. 2002 May;70(5):1368-75. doi: 10.1086/340390. Epub 2002 Apr 8. Am J Hum Genet. 2002. PMID: 11941538 Free PMC article.
43 results