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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1995 1
1996 1
1997 1
1998 1
2005 1
2011 1
2023 4
2024 1

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PubMed for id: 119709832

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Page 1
LRP5, Bone Mass Polymorphisms and Skeletal Disorders.
Littman J, Yang W, Olansen J, Phornphutkul C, Aaron RK. Littman J, et al. Genes (Basel). 2023 Sep 23;14(10):1846. doi: 10.3390/genes14101846. Genes (Basel). 2023. PMID: 37895195 Free PMC article. Review.
LRP5, SLC6A3, and SOX10 Expression in Conventional Ameloblastoma.
Correa-Arzate L, Portilla-Robertson J, Ramírez-Jarquín JO, Jacinto-Alemán LF, Mejía-Velázquez CP, Villanueva-Sánchez FG, Rodríguez-Vázquez M. Correa-Arzate L, et al. Genes (Basel). 2023 Jul 26;14(8):1524. doi: 10.3390/genes14081524. Genes (Basel). 2023. PMID: 37628576 Free PMC article.
Familial Exudative Vitreoretinopathy, Autosomal Dominant – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.
Toomes C, Downey L. Toomes C, et al. 2005 Mar 21 [updated 2011 Sep 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Mar 21 [updated 2011 Sep 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301326 Free Books & Documents. Review.
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.
Gong Y, Vikkula M, Boon L, Liu J, Beighton P, Ramesar R, Peltonen L, Somer H, Hirose T, Dallapiccola B, De Paepe A, Swoboda W, Zabel B, Superti-Furga A, Steinmann B, Brunner HG, Jans A, Boles RG, Adkins W, van den Boogaard MJ, Olsen BR, Warman ML. Gong Y, et al. Am J Hum Genet. 1996 Jul;59(1):146-51. Am J Hum Genet. 1996. PMID: 8659519 Free PMC article.