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111. Genetic and allelic heterogeneity in 248 Indians with skeletal dysplasia

120. Novel variants in the SOX11 gene: clinical description of seven new patients

148. De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India

150. Thickening fraction as a measure of ultrasonographic diaphragm dysfunction in amyotrophic lateral sclerosis

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