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Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9.

Congenital anomalies - 1 Sept 2020

Nishimura Naoto, Murakami Hiroaki, Hayashi Tomoko, Sato Hironobu, Kurosawa Kenji

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Share to Chromosomes, Human, Pair 9
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32277509
DOI: 10.1111/cga.12371

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Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9.PMID 32277509Read ↗

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