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107. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

110. SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

115. Imaging Infant Retinal Vasculature with OCT Angiography

119. Reply

134. Subretinal Hyperreflective Material in the Comparison of Age-Related Macular Degeneration Treatments Trials

138. The tools of data analysis: matching the hammer to the nail

142. Temporary Lumbar Drain as Treatment for Pediatric Fulminant Idiopathic Intracranial Hypertension.

144. Evaluation of Optic Nerve Development in Preterm and Term Infants Using Handheld Spectral-Domain Optical Coherence Tomography

148. Biallelic mutations in FDXR cause neurodegeneration associated with inflammation

149. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

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