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VP33.07: Use of whole‐exome sequencing in establishing diagnosis of a rare metabolic disorder manifesting with multiple anomalies in a fetus. (15th October 2020)
Record Type:
Journal Article
Title:
VP33.07: Use of whole‐exome sequencing in establishing diagnosis of a rare metabolic disorder manifesting with multiple anomalies in a fetus. (15th October 2020)
Main Title:
VP33.07: Use of whole‐exome sequencing in establishing diagnosis of a rare metabolic disorder manifesting with multiple anomalies in a fetus