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180 results

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Page 1
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.
Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, Bockenhauer D, Laing C, Walsh SB, McCredie DA, Povey S, Asselin A, Picard A, Coulomb A, Medlar AJ, Bailleul-Forestier I, Verloes A, Le Caignec C, Roussey G, Guiol J, Isidor B, Logan C, Shore R, Johnson C, Inglehearn C, Al-Bahlani S, Schmittbuhl M, Clauss F, Huckert M, Laugel V, Ginglinger E, Pajarola S, Spartà G, Bartholdi D, Rauch A, Addor MC, Yamaguti PM, Safatle HP, Acevedo AC, Martelli-Júnior H, dos Santos Netos PE, Coletta RD, Gruessel S, Sandmann C, Ruehmann D, Langman CB, Scheinman SJ, Ozdemir-Ozenen D, Hart TC, Hart PS, Neugebauer U, Schlatter E, Houillier P, Gahl WA, Vikkula M, Bloch-Zupan A, Bleich M, Kitagawa H, Unwin RJ, Mighell A, Berdal A, Kleta R. Jaureguiberry G, et al. Among authors: hart ps, hart tc. Nephron Physiol. 2012;122(1-2):1-6. doi: 10.1159/000349989. Epub 2013 Feb 23. Nephron Physiol. 2012. PMID: 23434854 Free PMC article.
A nomenclature for X-linked amelogenesis imperfecta.
Hart PS, Hart TC, Simmer JP, Wright JT. Hart PS, et al. Among authors: hart tc. Arch Oral Biol. 2002 Apr;47(4):255-60. doi: 10.1016/s0003-9969(02)00005-5. Arch Oral Biol. 2002. PMID: 11922868 Review.
Disorders of human dentin.
Hart PS, Hart TC. Hart PS, et al. Among authors: hart tc. Cells Tissues Organs. 2007;186(1):70-7. doi: 10.1159/000102682. Cells Tissues Organs. 2007. PMID: 17627120 Free PMC article.
Amelogenesis imperfecta: genotype-phenotype studies in 71 families.
Wright JT, Torain M, Long K, Seow K, Crawford P, Aldred MJ, Hart PS, Hart TC. Wright JT, et al. Among authors: hart ps, hart tc. Cells Tissues Organs. 2011;194(2-4):279-83. doi: 10.1159/000324339. Epub 2011 May 19. Cells Tissues Organs. 2011. PMID: 21597265 Free PMC article.
180 results