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scoliosis, idiopathic
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CHD7
Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and interfamilial variability
Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype
New recognized ophthalmic morphologic anomalies in CHARGE syndrome caused by the R2319C mutation in the CHD7 gene
Cancer Gene Census
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Definition
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