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Results 1 - 3 of 3 for Oxycephaly
  1. FGFR2 gene 
    ... Bonaventure J. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  2. Muenke syndrome 
    ... on the diagnosis and clinical management of syndromic craniosynostoses. Childs Nerv Syst. 2012 Sep;28(9):1447- ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  3. Jackson-Weiss syndrome 
    ... Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. Int J Pediatr ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics