Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation
Abstract Background Meier-Gorlin syndrome 7 (MGS7) is a rare autosomal recessive condition. We reported a fetus diagnosed with Meier-Gorlin syndrome 7. The antenatal sonographic images were presented, and compound heterozygous mutations of CDC45 on chromosome 22 were identified by whole-exome sequen...
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2021-05-01T00:00:00Z.
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