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Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.
J Clin Invest. 1997 Dec 1;100(11):2653-7. doi: 10.1172/JCI119809.
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New insights into the pathogenesis of inherited phosphate wasting disorders.
Bone. 1999 Jul;25(1):131-5. doi: 10.1016/s8756-3282(99)00108-8.
3
Multilocus mapping of the X-linked hypophosphatemic rickets gene.
J Clin Endocrinol Metab. 1992 Jul;75(1):201-6. doi: 10.1210/jcem.75.1.1352307.
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[Hereditary hypophosphatemia in adults].
Presse Med. 2005 Dec 17;34(22 Pt 1):1720-6. doi: 10.1016/s0755-4982(05)84260-5.
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Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.
Clin Endocrinol (Oxf). 1992 Oct;37(4):338-43. doi: 10.1111/j.1365-2265.1992.tb02335.x.
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Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23.
Kidney Int. 2001 Dec;60(6):2079-86. doi: 10.1046/j.1523-1755.2001.00064.x.
10
Flanking markers define the X-linked hypophosphatemic rickets gene locus.
J Bone Miner Res. 1993 Sep;8(9):1149-52. doi: 10.1002/jbmr.5650080916.

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Fibroblast Growth Factor 23 Bone Regulation and Downstream Hormonal Activity.
Calcif Tissue Int. 2023 Jul;113(1):4-20. doi: 10.1007/s00223-023-01092-1. Epub 2023 Jun 12.
2
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program.
J Bone Miner Res. 2022 Feb;37(2):202-214. doi: 10.1002/jbmr.4454. Epub 2021 Nov 10.
3
Usefulness of Ga-DOTATOC PET/CT to localize the culprit tumor inducing osteomalacia.
Sci Rep. 2021 Jan 19;11(1):1819. doi: 10.1038/s41598-021-81491-2.
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The Causes of Hypo- and Hyperphosphatemia in Humans.
Calcif Tissue Int. 2021 Jan;108(1):41-73. doi: 10.1007/s00223-020-00664-9. Epub 2020 Apr 13.
6
Regulation of Fibroblast Growth Factor 23 by Iron, EPO, and HIF.
Curr Mol Biol Rep. 2019 Mar;5(1):8-17. doi: 10.1007/s40610-019-0110-9. Epub 2019 Jan 25.
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Genetic Variants Associated with Circulating Fibroblast Growth Factor 23.
J Am Soc Nephrol. 2018 Oct;29(10):2583-2592. doi: 10.1681/ASN.2018020192. Epub 2018 Sep 14.
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The metabolic bone disease associated with the mutation is independent of osteoblastic HIF1α expression.
Bone Rep. 2017 Jan 17;6:38-43. doi: 10.1016/j.bonr.2017.01.003. eCollection 2017 Jun.
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Heritable and acquired disorders of phosphate metabolism: Etiologies involving FGF23 and current therapeutics.
Bone. 2017 Sep;102:31-39. doi: 10.1016/j.bone.2017.01.034. Epub 2017 Jan 31.
10
Coupling fibroblast growth factor 23 production and cleavage: iron deficiency, rickets, and kidney disease.
Curr Opin Nephrol Hypertens. 2014 Jul;23(4):411-9. doi: 10.1097/01.mnh.0000447020.74593.6f.

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Human stanniocalcin inhibits renal phosphate excretion in the rat.
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Human stanniocalcin: a possible hormonal regulator of mineral metabolism.
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A microsatellite genetic linkage map of human chromosome 18.
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Positional cloning moves from perditional to traditional.
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