Slater, Howard R.

Royal Children's Hospital · The University of Melbourne · Victorian Clinical Genetics Services · Murdoch Children's Research Institute

1 paper on CoChatORCID 0009-0000-3717-8724

Most cited papers

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Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature
Béna, F., Bruno, D. L., Eriksson, M., van Ravenswaaij‐Arts, C., Stark, Z., Dijkhuizen, T., Gerkes, E., Gimelli, S., Ganesamoorthy, D., Thuresson, A. C., et al. (2013) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
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