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Journal Abstract Search

174 related items for PubMed ID: 27485793

  • 21. New Magnetic Resonance Imaging (MRI) findings in a patient with hypochondroplasia caused by the FGFR3 N540K variant.
    Mimura PMP, Castro JTS, Jarry VM, França Júnior MC, Reis F.
    Arq Neuropsiquiatr; 2021 Jul; 79(7):656-657. PubMed ID: 34133497
    [No Abstract] [Full Text] [Related]

  • 22. Familial hypochondroplasia and acanthosis nigricans with FGFR3 K650T mutation.
    Cossiez Cacard MA, Coulombe J, Bernard P, Kaci N, Bressieux JM, Souchon PF, Motte J, Legeai-Mallet L, Hadj-Rabia S, Eschard C.
    J Eur Acad Dermatol Venereol; 2016 May; 30(5):897-8. PubMed ID: 25809207
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  • 23. Low bone mineral density in achondroplasia and hypochondroplasia.
    Matsushita M, Kitoh H, Mishima K, Kadono I, Sugiura H, Hasegawa S, Nishida Y, Ishiguro N.
    Pediatr Int; 2016 Aug; 58(8):705-8. PubMed ID: 26716907
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  • 28. Medial temporal lobe dysgenesis in hypochondroplasia.
    Kannu P, Hayes IM, Mandelstam S, Donnan L, Savarirayan R.
    Am J Med Genet A; 2005 Nov 01; 138(4):389-91. PubMed ID: 16222682
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  • 30. Familial acanthosis nigricans with the FGFR3 mutation: Differences of pigmentation between male and female patients.
    Yasuda M, Morimoto N, Shimizu A, Toyoshima T, Yokoyama Y, Ishikawa O.
    J Dermatol; 2018 Nov 01; 45(11):1357-1361. PubMed ID: 30168875
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  • 34. Further delineation of achondroplasia-hypochondroplasia complex with long-term survival.
    González-Del Angel A, Rius R, Alcántara-Ortigoza MA, Spector E, Del Castillo V, Mata-García LE.
    Am J Med Genet A; 2018 May 01; 176(5):1225-1231. PubMed ID: 29681095
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  • 38. Comparison of clinical, radiological and molecular findings in Korean infants and children with achondroplasia and hypochondroplasia.
    Shin YL, Choi JH, Kim GH, Yoo HW.
    J Pediatr Endocrinol Metab; 2005 Oct 01; 18(10):999-1005. PubMed ID: 16355813
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