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Journal Abstract Search

160 related items for PubMed ID: 15751611

  • 1. Novel growth hormone receptor mutation in a Chinese patient with Laron syndrome.
    Hui HN, Metherell LA, Ng KL, Savage MO, Camacho-Hübner C, Clark AJ.
    J Pediatr Endocrinol Metab; 2005 Feb; 18(2):209-13. PubMed ID: 15751611
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  • 4. Clinical features and growth hormone receptor gene mutations of patients with Laron syndrome from a Chinese family.
    Ying YQ, Wei H, Cao LZ, Lu JJ, Luo XP.
    Zhongguo Dang Dai Er Ke Za Zhi; 2007 Aug; 9(4):335-8. PubMed ID: 17706034
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  • 5. Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism.
    Arman A, Ozon A, Isguven PS, Coker A, Peker I, Yordam N.
    J Pediatr Endocrinol Metab; 2008 Jan; 21(1):47-58. PubMed ID: 18404972
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  • 7. Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous states.
    Fang P, Riedl S, Amselem S, Pratt KL, Little BM, Haeusler G, Hwa V, Frisch H, Rosenfeld RG.
    J Clin Endocrinol Metab; 2007 Jun; 92(6):2223-31. PubMed ID: 17405847
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  • 8. A novel exonic GHR splicing mutation (c.784G > C) in a patient with classical growth hormone insensitivity syndrome.
    Akıncı A, Rosenfeld RG, Hwa V.
    Horm Res Paediatr; 2013 Jun; 79(1):32-8. PubMed ID: 23006617
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  • 10. Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature.
    Guevara-Aguirre J, Rosenbloom AL, Guevara-Aguirre M, Yariz K, Saavedra J, Baumbach L, Shuster J.
    Growth Horm IGF Res; 2007 Jun; 17(3):261-4. PubMed ID: 17350302
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  • 15. Growth hormone (GH) insensitivity and insulin-like growth factor-I deficiency in Inuit subjects and an Ecuadorian cohort: functional studies of two codon 180 GH receptor gene mutations.
    Fang P, Girgis R, Little BM, Pratt KL, Guevara-Aguirre J, Hwa V, Rosenfeld RG.
    J Clin Endocrinol Metab; 2008 Mar; 93(3):1030-7. PubMed ID: 18073295
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  • 18. Novel growth hormone receptor gene mutation in a patient with Laron syndrome.
    Arman A, Yüksel B, Coker A, Sarioz O, Temiz F, Topaloglu AK.
    J Pediatr Endocrinol Metab; 2010 Apr; 23(4):407-14. PubMed ID: 20583548
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