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: Pfeiffer's syndrome family tree. Review of the literature.
    Author: Lyon JR, Burgess RC.
    Journal: Clin Orthop Relat Res; 1993 Sep; (294):294-8. PubMed ID: 8358932.
    Abstract:
    Pfeiffer's syndrome is an autosomal dominant disorder characterized by craniofacial abnormalities and distal extremity abnormalities. This case study reviews four generations of a family with craniofacial abnormalities, multiple simple syndactylies, and delta phalanges of bilateral great toes and thumbs inherited in an autosomal dominant fashion.
    [Abstract] [Full Text] [Related] [New Search]