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2010•European Journal of Medical GeneticsRequires access

Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1–q25.32: Genotype–phenotype correlations of chromosome 3q25 deletion syndrome

Stéphanie Moortgat, Christine Verellen‐Dumoulin, Isabelle Maystadt, Benoît Parmentier, Bernard Grisart, Jean-Luc Hennecker, Anne Destrèe

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Key concepts: Biology, Microcephaly, Genetics, Comparative genomic hybridization, Phenotype, Chromosome, Fluorescence in situ hybridization, Ptosis

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Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1–q25.32: Genotype–phenotype correlations of chromosome 3q25 deletion syndrome — Research Paper | ScholarLens