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

149 related items for PubMed ID: 16892303

  • 1. Sedaghatian spondylometaphyseal dysplasia with pachygyria and absence of the corpus callosum.
    English SJ, Gayatri N, Arthur R, Crow YJ.
    Am J Med Genet A; 2006 Sep 01; 140A(17):1854-8. PubMed ID: 16892303
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Spondylometaphyseal dysplasia: Sedaghatian type.
    Koutouby A, Habibullah J, Moinuddin FA.
    Am J Med Genet; 2000 Jan 31; 90(3):199-202. PubMed ID: 10678656
    [Abstract] [Full Text] [Related]

  • 4. Spondylometaphyseal dysplasia, Sedaghatian type.
    Peeden JN, Rimoin DL, Lachman RS, Dyer ML, Gerard D, Gruber HE.
    Am J Med Genet; 1992 Nov 15; 44(5):651-6. PubMed ID: 1481828
    [Abstract] [Full Text] [Related]

  • 5. Simplified gyral pattern with cerebellar hypoplasia in Sedaghatian type spondylometaphyseal dysplasia: a clinical report and review of the literature.
    Aygun C, Celik FC, Nural MS, Azak E, Kucukoduk S, Ogur G, Incesu L.
    Am J Med Genet A; 2012 Jun 15; 158A(6):1400-5. PubMed ID: 22529034
    [Abstract] [Full Text] [Related]

  • 6. A female case of Sedaghatian type spondylometaphyseal dysplasia.
    Foulds N, Fairhurst J, Temple IK, Cade S, Groves C, Lancaster T.
    Am J Med Genet A; 2003 May 01; 118A(4):377-81. PubMed ID: 12687672
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death.
    Sztriha L, Al-Gazali L, Dawodu A, Bakir M, Chandran P.
    Neurology; 1998 May 01; 50(5):1466-9. PubMed ID: 9596009
    [Abstract] [Full Text] [Related]

  • 10. Spondylometaphyseal dysplasia Sedaghatian type associated with lethal arrhythmia and normal intrauterine growth in three siblings.
    Kerr B, Smith V, Patel R, Ladusans E, Sillence DO.
    Clin Dysmorphol; 2000 Jul 01; 9(3):167-72. PubMed ID: 10955475
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Agenesis of the corpus callosum with mental retardation and osseous lesions.
    Kozlowski K, Ouvrier RA.
    Am J Med Genet; 1993 May 01; 48(1):6-9. PubMed ID: 8357037
    [Abstract] [Full Text] [Related]

  • 13. Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.
    Opitz JM, Spranger JW, Stöss HR, Pesch HJ, Azadeh B.
    Am J Med Genet; 1987 Mar 01; 26(3):583-90. PubMed ID: 3565474
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Spondylometaphyseal dysplasia: a variant form.
    Felman AH, Frias JL, Rennert OM.
    Radiology; 1974 Nov 01; 113(2):409-15. PubMed ID: 4419008
    [No Abstract] [Full Text] [Related]

  • 16. Congenital hypothyroidism presenting as apparent spondyloepiphyseal dysplasia.
    Eberle AJ.
    Am J Med Genet; 1993 Sep 15; 47(4):464-7. PubMed ID: 8256805
    [Abstract] [Full Text] [Related]

  • 17. Morphometric variability of neuroimaging features in children with agenesis of the corpus callosum.
    Neal JB, Filippi CG, Mayeux R.
    BMC Neurol; 2015 Jul 25; 15():116. PubMed ID: 26209096
    [Abstract] [Full Text] [Related]

  • 18. Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome?
    Schinzel A.
    Helv Paediatr Acta; 1979 May 25; 34(2):141-6. PubMed ID: 457430
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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