K. Hernandez

De novo deletion of TBL1XR1 in a child with non‐specific developmental delay supports its implication in intellectual disability

A. Verloes, B. Benzacken, C. Dupont, 2014, American journal of medical genetics. Part A.

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations

I Scala, Alain Verloes, M. Elmaleh, 2009, Neurology.

Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory

W. Huttner, P. Gressens, S. Eliez, 2016, Cortex.

GJB2 Variants and Auditory Outcomes among Filipino Cochlear Implantees

R. Santos-Cortez, E. M. Cutiongco-de la Paz, C. Chiong, 2013, Audiology and Neurotology Extra.