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Incidence and clinical features of X-linked Cornelia de Lange syndrome due toSMC1L1 mutations

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Academic year: 2021

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Figure

Figure 2. Photographs of patients 1 (A) and 2 (B) showing dysmorphic features of CdLS caused by SMC1L1  mutations
Table 1. Results of Genotype-Phenotype Correlation Analysis in CdLS Patients Carrying SMC1L1 or NIPBL Mutations

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