Phelan, K.

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)

Phelan, K., & McDermid, H. E. (2011) · Molecular Syndromology

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Redin, C., Brand, H., Collins, R. L., Kammin, T., Mitchell, E., Hodge, J. C., Hanscom, C., Pillalamarri, V., Seabra, C. M., Abbott, M.-A., et al. (2017) · Nature Genetics

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

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