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

Search MEDLINE/PubMed

  • Title: Van der Woude syndrome.
    Author: Guner U, Celik N, Ozek C, Cagdas A.
    Journal: Scand J Plast Reconstr Surg Hand Surg; 2002; 36(2):103-5. PubMed ID: 12038200.
    Abstract:
    Van der Woude syndrome (VWS) is an autosomal dominant craniofacial syndrome with variable expression characterised by congenital pits and sinuses in the lower lip together with cleft lip, or palate, or both. We report a case of VWS, which occurred as a new mutation, and review previous reports.
    [Abstract] [Full Text] [Related] [New Search]