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 Craniofacial Anomalies
 Directory > Health > Diseases and Conditions > Craniofacial Anomalies
 
 
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  • American Cleft Palate-Craniofacial Association Open site in a new window - National organisation providing lay and professional services for cleft lip, cleft palate and other craniofacial deformities.
  • Australasian Cleft Lip and Palate Association (ACLAPA) Open site in a new window - Representing the interests of health professionals involved in the management of cleft lip and palate related conditions.
  • Cleft Advocate Open site in a new window - Nonprofit organisation providing extensive educational and support resources for cleft lip/palate. Includes insurance and advocacy information and on-line family networking.
  • Cleft Club Open site in a new window - Cleft lip and cleft palate support group for those born cleft and parents of cleft children. Includes mailing lists, message boards, chat, news, and more.
  • Cleft Support Open site in a new window - Support and information for individuals and families affected by cleft lip and/or palate. Includes personal stories, links, pictures, and information.
  • Craniofacial Foundation of Arizona Open site in a new window - Dedicated to providing financial and emotional support to patients and their families.
  • FACES Open site in a new window - Provides information, support, resources, and financial assistance for persons with craniofacial disorders.
  • Headlines Open site in a new window - Supports the following conditions, Apert Syndrome, Crouzon syndrome, Pfeiffer syndrome, Saethre-Chotzen syndrome, and single suture craniosynostosis.
  • International Craniofacial Institute Open site in a new window - Provides treatment for craniofacial deformities, syndromes, trauma, and cleft lip and palate conditions.
  • Let's Face It Open site in a new window - Information about resources and networks relate to craniofacial anomalies.
  • MUSC Craniofacial Anomalies and Cleft Palate Center Open site in a new window - The Craniofacial Anomalies and Cleft Palate Centre at the Medical University of South Carolina provides optimal care services for patients with cleft lip and palate and other craniofacial anomalies through an interdisciplinary team approach.
  • Pierre Robin Network Open site in a new window - Group of parents seeking to network with others looking for information and support on Pierre Robin Syndrome/Sequence.
  • Smiles Open site in a new window - Support group dedicated to improve the lives of children with cleft lip, cleft palate, and/or craniofacial deformities.
  • WideSmiles Open site in a new window - Nonprofit organisation providing resources, support, and information for those affected by cleft lip/palate, the fourth most common birth defect.
 



 
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