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

133 related items for PubMed ID: 23401300

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

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

  • 3. Brachytelephalangic chondrodysplasia punctata: prenatal diagnosis and postnatal outcome.
    Boulet S, Dieterich K, Althuser M, Nugues F, Durand C, Charra C, Schaal JP, Jouk PS.
    Fetal Diagn Ther; 2010; 28(3):186-90. PubMed ID: 20523025
    [Abstract] [Full Text] [Related]

  • 4. Radiological picture of premature baby with manifestation of brachytelephalangic type chondrodysplasia punctata, myelomalacia.
    Koç U, Karakaş P.
    Turk J Pediatr; 2017; 59(5):604-609. PubMed ID: 29745127
    [Abstract] [Full Text] [Related]

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

  • 6. Brachytelephalangic chondrodysplasia punctata.
    Bieganski T, Kozlowski K.
    Australas Radiol; 1998 Aug; 42(3):244-5. PubMed ID: 9727255
    [Abstract] [Full Text] [Related]

  • 7. Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?
    Mortier GR, Messiaen LM, Espeel M, Smets KJ, Vanzieleghem BD, Roels F, De Paepe AM.
    Pediatr Radiol; 1998 Oct; 28(10):790-3. PubMed ID: 9799302
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of brachytelephalangic chondrodysplasia punctata: case report.
    Benaicha A, Dommergues M, Jouannic JM, Jacquette A, Alexandre M, Le Merrer M, Ducou Le Pointe H, Garel C.
    Ultrasound Obstet Gynecol; 2009 Dec; 34(6):724-6. PubMed ID: 19856318
    [Abstract] [Full Text] [Related]

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

  • 10. Clinical and genetic analysis of a Korean patient with X-linked chondrodysplasia punctata: identification of a novel splicing mutation in the ARSE gene.
    Jeon GW, Kwon MJ, Lee SJ, Sin JB, Ki CS.
    Ann Clin Lab Sci; 2013 Dec; 43(1):70-5. PubMed ID: 23462608
    [Abstract] [Full Text] [Related]

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

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

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

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

  • 17. Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX).
    Savarirayan R.
    Pediatr Radiol; 1999 May; 29(5):322. PubMed ID: 10382206
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No 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 7.