JANE EDMOND to Mutation
This is a "connection" page, showing publications JANE EDMOND has written about Mutation.
Connection Strength
0.107
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Mitochondrial disorders. Int Ophthalmol Clin. 2009; 49(3):27-33.
Score: 0.030
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Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations. J AAPOS. 2006 Dec; 10(6):521-7.
Score: 0.026
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Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome. AJNR Am J Neuroradiol. 2023 02; 44(2):212-217.
Score: 0.020
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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.
Score: 0.017
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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.
Score: 0.013