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

Journal Abstract Search


120 related items for PubMed ID: 6859106

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Cerebral abnormalities in the Neu-Laxova syndrome.
    Ostrovskaya TI, Lazjuk GI.
    Am J Med Genet; 1988 Jul; 30(3):747-56. PubMed ID: 3055985
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome?
    Orstavik KH, Strömme P, Spetalen S, Flage T, Westvik J, Vesterhus P, Skjeldal O.
    Am J Med Genet; 1995 Oct 23; 59(1):92-5. PubMed ID: 8849019
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Bilateral microphthalmia with cyst, facial clefts, and limb anomalies: a new syndrome with features of Waardenburg syndrome, cerebro-oculo-nasal syndrome, and craniotelencephalic dysplasia.
    Gupta PC, Peralta D, Parker M, Crowe C, Clark B, Traboulsi EI.
    Am J Med Genet A; 2003 Feb 15; 117A(1):72-5. PubMed ID: 12548743
    [Abstract] [Full Text] [Related]

  • 14. Further delineation of the Baller-Gerold syndrome.
    Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ.
    Am J Med Genet; 1993 Feb 15; 45(4):519-24. PubMed ID: 8465861
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull.
    Saal HM, Bulas DI, Allen JF, Vezina LG, Walton D, Rosenbaum KN.
    Am J Med Genet; 1995 Jul 17; 57(4):573-8. PubMed ID: 7573131
    [Abstract] [Full Text] [Related]

  • 18. Fryns syndrome survivors and neurologic outcome.
    Van Hove JL, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla AK, Kahler SG.
    Am J Med Genet; 1995 Nov 20; 59(3):334-40. PubMed ID: 8599357
    [Abstract] [Full Text] [Related]

  • 19. Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia.
    Miyata H, Chute DJ, Fink J, Villablanca P, Vinters HV.
    Acta Neuropathol; 2004 Jan 20; 107(1):69-81. PubMed ID: 14566414
    [Abstract] [Full Text] [Related]

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


    Page: [Next] [New Search]
    of 6.