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Asli Silahtaroglu

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Human Molecular Genetics|July 3, 2014

Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxiaSheroy Minocherhomji, Claus Hansen, Hyung-Goo Kim, et al.

Epilepsia|November 21, 2014

Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-convergence on axonal guidanceSanne S Kaalund, Morten T Venø, Mads Bak, et al.

American Journal of Human Genetics|May 29, 2018

Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term OutcomesChristina Halgren, Nete M Nielsen, Lusine Nazaryan-Petersen, et al.

Biological Psychiatry|October 8, 2015

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European CohortBirgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, et al.

American Journal of Human Genetics|July 10, 2012

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomaliesHyung-Goo Kim, Hyun-Taek Kim, Natalia T Leach, et al.

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Search research articles

Showing results (31-40 of 35) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 35 results.

Human Molecular Genetics|July 3, 2014

Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxiaSheroy Minocherhomji, Claus Hansen, Hyung-Goo Kim, et al.

Epilepsia|November 21, 2014

Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-convergence on axonal guidanceSanne S Kaalund, Morten T Venø, Mads Bak, et al.

American Journal of Human Genetics|May 29, 2018

Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term OutcomesChristina Halgren, Nete M Nielsen, Lusine Nazaryan-Petersen, et al.

Biological Psychiatry|October 8, 2015

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European CohortBirgitte Bertelsen, Hreinn Stefánsson, Lars Riff Jensen, et al.

American Journal of Human Genetics|July 10, 2012

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomaliesHyung-Goo Kim, Hyun-Taek Kim, Natalia T Leach, et al.

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