Article

3q27.1 Microdeletion Causes a Clinically Recognizable Syndrome Characterized by Severe Prenatal and Postnatal Growth Restriction and Neurodevelopmental Abnormalities

2021-09-02

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold>Constitutional deletions/rearrangements involving chromosome 3q are uncommon and overlapping microdeletions of chromosome 3q26-3q28 have only been reported in eight individuals. The common phenotype observed in these individuals include severe intrauterine growth restriction and postnatal growth impairment, feeding difficulties, characteristic facial features, fee...

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Literature Corpus work: b7477af6-0a11-5109-8e92-f7730f821e96
DOI: 10.21203/rs.3.rs-853179/v1

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