Connection

JANE EDMOND to Mutation

This is a "connection" page, showing publications JANE EDMOND has written about Mutation.
Connection Strength

0.107
  1. Mitochondrial disorders. Int Ophthalmol Clin. 2009; 49(3):27-33.
    View in: PubMed
    Score: 0.030
  2. Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations. J AAPOS. 2006 Dec; 10(6):521-7.
    View in: PubMed
    Score: 0.026
  3. Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. AJNR Am J Neuroradiol. 2023 02; 44(2):212-217.
    View in: PubMed
    Score: 0.020
  4. Phenotypic expansion of Bosch-Boonstra-Schaaf optic atrophy syndrome and further evidence for genotype-phenotype correlations. Am J Med Genet A. 2020 06; 182(6):1426-1437.
    View in: PubMed
    Score: 0.017
  5. An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a TUBB3 mutation. Cold Spring Harb Mol Case Stud. 2017 03; 3(2):a000984.
    View in: PubMed
    Score: 0.013
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.