Pino J. Poddighe

Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome

B. D. de Vries, L. Koster, B. Oostra, 2013, American journal of medical genetics. Part A.

Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature

N. de Leeuw, T. Kleefstra, C. V. van Ravenswaaij-Arts, 2010, American journal of medical genetics. Part A.

Abnormalities of chromosome 1p/q are highly associated with chromosome 13/13q deletions and are an adverse prognostic factor for the outcome of high‐dose chemotherapy in patients with multiple myeloma

P. Sonneveld, B. van der Holt, G. Verhoef, 2007, British journal of haematology.

Interphase cytogenetics of tumours

F. Ramaekers, A. Hopman, F C Ramaekers, 1992, The Journal of pathology.