Article

3q29 Microduplication syndrome: a new family case of phenotype heterogeneity

2022-07-13

Abstract excerpt

Here, we describe a family case carrier with 3q29 microduplication, a 1.56Mb and 1.68 Mb duplicate region, that was identified by CNV-seq. Different from the common clinical traits of previously reported cases, this family of individuals shows an apparently normal phenotype.

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Literature Corpus work: 8dc2340d-3169-5760-a57e-10f5fcfeddd6
DOI: 10.22541/au.165771211.12582203/v1

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