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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

146 related items for PubMed ID: 2063920

  • 1. Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfecta.
    Goldblatt J, Carman P, Sprague P.
    Am J Med Genet; 1991 May 01; 39(2):170-2. PubMed ID: 2063920
    [Abstract] [Full Text] [Related]

  • 2. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL): a Brazilian case.
    Pina-Neto JM, Defino HL, Guedes ML, Jorge SM.
    Am J Med Genet; 1996 Jan 11; 61(2):131-3. PubMed ID: 8669438
    [Abstract] [Full Text] [Related]

  • 3. Spondyloepimetaphyseal dysplasia (SEMD) Shohat type.
    Figuera LE, Ramírez-Dueñas ML, Gallegos-Arreola MP, Cantú JM.
    Am J Med Genet; 1994 Jul 01; 51(3):213-5. PubMed ID: 8074146
    [Abstract] [Full Text] [Related]

  • 4. The manifestations and natural history of spondylo-epi-metaphyseal dysplasia with joint laxity.
    Beighton P, Gericke G, Kozlowski K, Grobler L.
    Clin Genet; 1984 Oct 01; 26(4):308-17. PubMed ID: 6499247
    [Abstract] [Full Text] [Related]

  • 5. Heritable bone fragility, joint laxity and dysplastic dentin in Friesian calves: a bovine syndrome of osteogenesis imperfecta.
    Denholm LJ, Cole WG.
    Aust Vet J; 1983 Jan 01; 60(1):9-17. PubMed ID: 6830550
    [Abstract] [Full Text] [Related]

  • 6. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL) in three neonates.
    Christianson AL, Beighton P.
    Genet Couns; 1996 Jan 01; 7(3):219-25. PubMed ID: 8897044
    [Abstract] [Full Text] [Related]

  • 7. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL): clinical and radiological findings in a Guatemalan patient.
    Bradburn JM, Hall BD.
    Am J Med Genet; 1995 Nov 06; 59(2):234-7. PubMed ID: 8588592
    [Abstract] [Full Text] [Related]

  • 8. Costello syndrome: a postnatal growth retardation syndrome with distinct phenotype.
    Fryns JP, Vogels A, Haegeman J, Eggermont E, van den Berghe H.
    Genet Couns; 1994 Nov 06; 5(4):337-43. PubMed ID: 7888135
    [Abstract] [Full Text] [Related]

  • 9. Dentinogenesis imperfecta.
    Goodman DB.
    Int J Orthod; 1973 Mar 06; 11(1):11-6. PubMed ID: 4512282
    [No Abstract] [Full Text] [Related]

  • 10. [Mesomelic dwarfism. Pronounced form in a female infant of a father with dyschondrosteosis and a mother with Madelung's deformity].
    Gugliantini P, Scapaticci A.
    Radiol Med; 1978 Apr 06; 64(4):433-44. PubMed ID: 704970
    [Abstract] [Full Text] [Related]

  • 11. [Occurrence of dentinogenesis imperfecta hereditaria (Capdepont's disease) in four successive generations of one family].
    Szczepanński M, Uścinowicz M, Kaczmarski M.
    Pediatr Pol; 1995 Aug 06; 70(8):679-81. PubMed ID: 8668371
    [Abstract] [Full Text] [Related]

  • 12. A syndrome of skeletal dysplasia, joint laxity, and mental retardation.
    Katsantoni A, Côté GB.
    Prog Clin Biol Res; 1982 Aug 06; 104():155-6. PubMed ID: 7163259
    [No Abstract] [Full Text] [Related]

  • 13. Spondyloepimetaphyseal dysplasia with joint laxity (Beighton type): A unique South African disorder.
    Honey EM.
    S Afr Med J; 2016 May 25; 106(6 Suppl 1):S54-6. PubMed ID: 27245527
    [Abstract] [Full Text] [Related]

  • 14. [Monographic study on dentinogenesis imperfecta].
    Iñiguez CT.
    An Esp Odontoestomatol; 1967 May 25; 26(3):240-8. PubMed ID: 5233970
    [No Abstract] [Full Text] [Related]

  • 15. Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?
    Moog U, Maroteaux P, Schrander-Stumpel CT, van Ooij A, Schrander JJ, Fryns JP.
    J Med Genet; 1999 Nov 25; 36(11):856-8. PubMed ID: 10544232
    [Abstract] [Full Text] [Related]

  • 16. [Problems in dentinogenesis imperfecta].
    Hrdinová V, Tachovská A, Zizka J.
    Cesk Stomatol; 1976 Sep 25; 76(5):346-52. PubMed ID: 1068752
    [No Abstract] [Full Text] [Related]

  • 17. Bone dysplasia in a child born to parents with osteogenesis imperfecta and pseudoachondroplasia.
    Kitoh H, Oki T, Arao K, Nogami H.
    Am J Med Genet; 1994 Jul 01; 51(3):187-90. PubMed ID: 8074142
    [Abstract] [Full Text] [Related]

  • 18. Radiographic features of spondylo-epimetaphyseal dysplasia with joint laxity and progressive kyphoscoliosis. Review of 19 cases.
    Kozlowski K, Beighton P.
    Rofo; 1984 Sep 01; 141(3):337-41. PubMed ID: 6435203
    [Abstract] [Full Text] [Related]

  • 19. Spondylometaphyseal dysplasia (Kozlowski type): case report.
    Guzman CM, Aaron GR.
    Pediatr Dent; 1993 Sep 01; 15(1):49-52. PubMed ID: 8233993
    [Abstract] [Full Text] [Related]

  • 20. Pseudoachondroplastic dysplasia.
    Khungar A, Mahajan P, Gupte G, Vasundhara M, Kher A, Bharucha BA.
    J Postgrad Med; 1993 Sep 01; 39(2):91-3. PubMed ID: 8169872
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.