These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 4283754)

  • 61. [Epiphysial dysplasia; a proteiform entity].
    SILVERMAN FN
    Ann Radiol (Paris); 1961; 4():833-67. PubMed ID: 13912929
    [No Abstract]   [Full Text] [Related]  

  • 62. Rapidly progressive scoliosis in multiple epiphyseal dysplasia. A case report.
    Herring JA
    J Bone Joint Surg Am; 1976 Jul; 58(5):703-4. PubMed ID: 932068
    [No Abstract]   [Full Text] [Related]  

  • 63. New pathogenic variant in the NPR2 gene: Etiology of low size, macrocephaly and bone dysplasia in a male with acromesomelic dysplasia Maroteaux-type.
    Vera Sáez-Benito MC; Izquierdo-Álvarez S; de Arriba Muñoz A
    Med Clin (Barc); 2017 Dec; 149(12):553-554. PubMed ID: 28736064
    [No Abstract]   [Full Text] [Related]  

  • 64. [Angel-shaped phalango-epiphyseal dysplasia: case report].
    Conci R; Oller A; Moya M; Echegaray A; Frush D
    Arch Argent Pediatr; 2017 Feb; 115(1):e1-e4. PubMed ID: 28097844
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Dysplasia epiphysialis hemimelica (tarso-ephiphysial aclasis).
    FAIRBANK TJ
    J Bone Joint Surg Br; 1956 Feb; 38-B(1):237-57. PubMed ID: 13295331
    [No Abstract]   [Full Text] [Related]  

  • 66. Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al.
    Kantaputra PN
    Am J Med Genet A; 2004 Jul; 128A(1):1-5. PubMed ID: 15211646
    [No Abstract]   [Full Text] [Related]  

  • 67. Floating-Harbor syndrome.
    Patton MA; Hurst J; Donnai D; McKeown CM; Cole T; Goodship J
    J Med Genet; 1991 Mar; 28(3):201-4. PubMed ID: 2051457
    [No Abstract]   [Full Text] [Related]  

  • 68. An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs.
    Moravej H; Moghtaderi M; Mostafavi S
    J Clin Res Pediatr Endocrinol; 2020 Mar; 12(1):122-123. PubMed ID: 31339259
    [No Abstract]   [Full Text] [Related]  

  • 69. Punctuate epiphyseal dysplasia.
    LIGHTWOOD R
    Proc R Soc Med; 1951 Mar; 44(3):227. PubMed ID: 14834199
    [No Abstract]   [Full Text] [Related]  

  • 70. [Congenital multiple punctate epiphyseal dysplasia].
    GINGOL'D AI; IVANOVA LI
    Vestn Rentgenol Radiol; 1962; 37():63-5. PubMed ID: 13898743
    [No Abstract]   [Full Text] [Related]  

  • 71. Hereditary multiple epiphysial dysplasia.
    Hoefnagel D; Sycamore LK; Russell SW; Bucknall WE
    Ann Hum Genet; 1967 Jan; 30(3):201-10. PubMed ID: 6032004
    [No Abstract]   [Full Text] [Related]  

  • 72. Non-traditional forms of inheritance in skeletal dysplasias.
    Hall JG; Lopez-Rangel E
    Pediatr Radiol; 1994; 24(6):407-9. PubMed ID: 7700715
    [No Abstract]   [Full Text] [Related]  

  • 73. Expanding the phenotype of SETD5-related disorder and presenting a novel association with bone fragility.
    Anderson E; Lam Z; Arundel P; Parker M; Balasubramanian M
    Clin Genet; 2021 Sep; 100(3):352-354. PubMed ID: 34169511
    [No Abstract]   [Full Text] [Related]  

  • 74. Experiences with epiphyseal arrest in correcting discrepancies in length of the lower extremities in infantile paralysis; a method of predicting the effect.
    GREEN WT; ANDERSON M
    J Bone Joint Surg Am; 1947 Jul; 29(3):659-75. PubMed ID: 20253040
    [No Abstract]   [Full Text] [Related]  

  • 75. [Dysplasia epiphysialis multiplex (of the Ribbing-Fairbank type)].
    Kozlowski K; Rokosz A
    Pediatr Pol; 1969 Oct; 44(10):1305-8. PubMed ID: 5351549
    [No Abstract]   [Full Text] [Related]  

  • 76. Craniofrontonasal dysplasia: genetic heterogeneity?
    Kwee ML; Lindhout D
    Clin Genet; 1984 Jul; 26(1):80. PubMed ID: 6467664
    [No Abstract]   [Full Text] [Related]  

  • 77. Dysplasia epiphysialis multiplex: a case report and review of the literature.
    Berg PK
    Am J Roentgenol Radium Ther Nucl Med; 1966 May; 97(1):31-8. PubMed ID: 5938048
    [No Abstract]   [Full Text] [Related]  

  • 78. Pachydermoperiostosis: scintigraphic, thermographic, plethysmographic, and capillaroscopic observations.
    Fam AG; Chin-Sang H; Ramsay CA
    Ann Rheum Dis; 1983 Feb; 42(1):98-102. PubMed ID: 6830331
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Multiple epiphyseal dysplasia. Report of a pedigree.
    Murphy MC; Shine IB; Stevens DB
    J Bone Joint Surg Am; 1973 Jun; 55(4):814-20. PubMed ID: 4283754
    [No Abstract]   [Full Text] [Related]  

  • 80. Acrocapitofemoral dysplasia: an autosomal recessive skeletal dysplasia with cone shaped epiphyses in the hands and hips.
    Mortier GR; Kramer PP; Giedion A; Beemer FA
    J Med Genet; 2003 Mar; 40(3):201-7. PubMed ID: 12624140
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.