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Article

Who ever heard of 16p11.2 deletion syndrome? Parents’ perspectives on a susceptibility copy number variation syndrome

15 May 2020

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Share to Genomic variations and chromosomal abnormalities
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32415274
DOI: 10.1038/s41431-020-0644-6

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Who ever heard of 16p11.2 deletion syndrome? Parents’ perspectives on a susceptibility copy number variation syndromePMID 32415274Read ↗

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Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV.Semantic proximity Read ↗

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Frequency and predictive value of 22q11 deletion.Semantic proximity Read ↗

A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: is this a candidate region for the syndrome?Semantic proximity Read ↗

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