Apert syndrome diagnosed by prenatal ultrasound combined with magnetic resonance imaging and whole exome sequencing: A case report

doi:10.12998/wjcc.v9.i4.912

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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Case Report

World J Clin Cases. Feb 6, 2021; 9(4): 912-918
Published online Feb 6, 2021. doi: 10.12998/wjcc.v9.i4.912

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Figure 5 Schematic diagram of Sanger sequencing verification results of the tested subject and parents with FGFR2 gene variation (whole exome sequencing was performed at Hangzhou Jinnuo Medical Laboratory).

Citation: Chen L, Huang FX. Apert syndrome diagnosed by prenatal ultrasound combined with magnetic resonance imaging and whole exome sequencing: A case report. World J Clin Cases 2021; 9(4): 912-918
URL: https://www.wjgnet.com/2307-8960/full/v9/i4/912.htm
DOI: https://dx.doi.org/10.12998/wjcc.v9.i4.912

Chen L, Huang FX. Apert syndrome diagnosed by prenatal ultrasound combined with magnetic resonance imaging and whole exome sequencing: A case report. World J Clin Cases 2021; 9(4): 912-918 [PMID: 33585639 DOI: 10.12998/wjcc.v9.i4.912]

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