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162 related items for PubMed ID: 32963591

  • 1. Description of a novel SLC34A3.c.671delT mutation causing hereditary hypophosphatemic rickets with hypercalciuria in two adolescent boys and response to recombinant human growth hormone.
    Dreimane D, Chen A, Bergwitz C.
    Ther Adv Musculoskelet Dis; 2020; 12():1759720X20912862. PubMed ID: 32963591
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  • 9. SLC34A3 intronic deletion in a new kindred with hereditary hypophosphatemic rickets with hypercalciuria.
    Hasani-Ranjbar S, Amoli MM, Ebrahim-Habibi A, Dehghan E, Soltani A, Amiri P, Larijani B.
    J Clin Res Pediatr Endocrinol; 2012 Jun; 4(2):89-93. PubMed ID: 22672866
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  • 15. Growth hormone therapy in HHRH.
    Filler G, Schott C, Salerno FR, Ens A, McIntyre CW, Díaz González de Ferris ME, Stein R.
    Bone Rep; 2022 Jun; 16():101591. PubMed ID: 35663378
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  • 17. SLC34A3 Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria.
    Hasani-Ranjbar S, Ejtahed HS, Amoli MM, Bitarafan F, Qorbani M, Soltani A, Yarjoo B.
    J Clin Res Pediatr Endocrinol; 2018 Nov 29; 10(4):343-349. PubMed ID: 29809158
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