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	21.	Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome. [electronic resource] by Maynard, Thomas M Horvath, Anelia Bernot, James P Karpinski, Beverly A Tavares, Andre L P Shah, Ankita Zheng, Qianqian Spurr, Liam Olender, Jacqueline Moody, Sally A Fraser, Claire M LaMantia, Anthony-S Lee, Norman H Publication details: Human molecular genetics 06 2020 In: Human molecular genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome. [electronic resource] by Maynard, Thomas M Horvath, Anelia Bernot, James P Karpinski, Beverly A Tavares, Andre L P Shah, Ankita Zheng, Qianqian Spurr, Liam Olender, Jacqueline Moody, Sally A Fraser, Claire M LaMantia, Anthony-S Lee, Norman H Producer: 20210705 In: Human molecular genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment. [electronic resource] by Fernandez, Alejandra Meechan, Daniel W Karpinski, Beverly A Paronett, Elizabeth M Bryan, Corey A Rutz, Hanna L Radin, Eric A Lubin, Noah Bonner, Erin R Popratiloff, Anastas Rothblat, Lawrence A Maynard, Thomas M LaMantia, Anthony-Samuel Producer: 20200323 In: Neuron vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Developmental and degenerative features in a complicated spastic paraplegia. [electronic resource] by Manzini, M Chiara Rajab, Anna Maynard, Thomas M Mochida, Ganeshwaran H Tan, Wen-Hann Nasir, Ramzi Hill, R Sean Gleason, Danielle Al Saffar, Muna Partlow, Jennifer N Barry, Brenda J Vernon, Mike LaMantia, Anthony-Samuel Walsh, Christopher A Producer: 20100514 In: Annals of neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome. [electronic resource] by Manzini, M Chiara Tambunan, Dimira E Hill, R Sean Yu, Tim W Maynard, Thomas M Heinzen, Erin L Shianna, Kevin V Stevens, Christine R Partlow, Jennifer N Barry, Brenda J Rodriguez, Jacqueline Gupta, Vandana A Al-Qudah, Abdel-Karim Eyaid, Wafaa M Friedman, Jan M Salih, Mustafa A Clark, Robin Moroni, Isabella Mora, Marina Beggs, Alan H Gabriel, Stacey B Walsh, Christopher A Producer: 20121217 In: American journal of human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)