Willatt, Lionel

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Mefford, H. C., Sharp, A. J., Baker, C., Itsara, A., Jiang, Z., Buysse, K., Huang, S., Maloney, V. K., Crolla, J. A., Baralle, D., et al. (2008) · New England Journal of Medicine

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

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Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder

Clayton-Smith, J., Giblin, C., Smith, R. A., Dunn, C., & Willatt, L. (2010) · Clinical Dysmorphology

Genomic variations and chromosomal abnormalitiesBipolar Disorder and Treatment

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