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

533 related items for PubMed ID: 20859208

  • 1. Holoprosencephaly: recommendations for diagnosis and management.
    Kauvar EF, Muenke M.
    Curr Opin Pediatr; 2010 Dec; 22(6):687-95. PubMed ID: 20859208
    [Abstract] [Full Text] [Related]

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

  • 3. Etiopathogenetic advances and management of holoprosencephaly: from bench to bedside.
    Bellone S, De Rienzo F, Prodam F, Savastio S, Busti A, Genoni G, Aimaretti G, Bona G.
    Panminerva Med; 2010 Dec; 52(4):345-54. PubMed ID: 21183895
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 7. Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
    Winter TC, Kennedy AM, Woodward PJ.
    Radiographics; 2015 Dec; 35(1):275-90. PubMed ID: 25590404
    [Abstract] [Full Text] [Related]

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

  • 9. Molecular testing in holoprosencephaly.
    Kruszka P, Martinez AF, Muenke M.
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):187-193. PubMed ID: 29771000
    [Abstract] [Full Text] [Related]

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

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

  • 12. Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans.
    Petryk A, Graf D, Marcucio R.
    Wiley Interdiscip Rev Dev Biol; 2015 Jun; 4(1):17-32. PubMed ID: 25339593
    [Abstract] [Full Text] [Related]

  • 13. Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE.
    Rosenfeld JA, Ballif BC, Martin DM, Aylsworth AS, Bejjani BA, Torchia BS, Shaffer LG.
    Hum Genet; 2010 Apr; 127(4):421-40. PubMed ID: 20066439
    [Abstract] [Full Text] [Related]

  • 14. Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.
    Kauvar EF, Solomon BD, Curry CJ, van Essen AJ, Janssen N, Dutra A, Roessler E, Muenke M.
    Am J Med Genet C Semin Med Genet; 2010 Feb 15; 154C(1):158-69. PubMed ID: 20104613
    [Abstract] [Full Text] [Related]

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

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

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Rescue of holoprosencephaly in fetal alcohol-exposed Cdon mutant mice by reduced gene dosage of Ptch1.
    Hong M, Krauss RS.
    PLoS One; 2013 Feb 15; 8(11):e79269. PubMed ID: 24244464
    [Abstract] [Full Text] [Related]

  • 19. Management of children with holoprosencephaly.
    Levey EB, Stashinko E, Clegg NJ, Delgado MR.
    Am J Med Genet C Semin Med Genet; 2010 Feb 15; 154C(1):183-90. PubMed ID: 20104615
    [Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 27.