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Microcephaly and Chorioretinopathy 1
A syndrome that is characterized by delayed psychomotor development and visual impairment, often accompanied by short stature and is caused by homozygous or compound heterozygous mutation in the TUBGCP6 gene.
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Overview
A syndrome that is characterized by delayed psychomotor development and visual impairment, often accompanied by short stature and is caused by homozygous or compound heterozygous mutation in the TUBGCP6 gene.
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