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Laura Vandenhove

Katholieke Universiteit Leuven

4

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The clinical relevance of intragenic NRXN1 deletions

2020 Journal of Medical Genetics
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ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder

2018 European Journal of Medical Genetics
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The clinical relevance of intragenic NRXN1 deletions

2017
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ZNF462 mutations cause syndromic intellectual disability with ptosis and distinct craniofacial anomalies

2017
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