Your search returned 2 results.

Results
	1.	A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay. [electronic resource] by Mucha, Bettina E Banka, Siddharth Ajeawung, Norbert Fonya Molidperee, Sirinart Chen, Gary G Koenig, Mary Kay Adejumo, Rhamat B Till, Marianne Harbord, Michael Perrier, Renee Lemyre, Emmanuelle Boucher, Renee-Myriam Skotko, Brian G Waxler, Jessica L Thomas, Mary Ann Hodge, Jennelle C Gecz, Jozef Nicholl, Jillian McGregor, Lesley Linden, Tobias Sisodiya, Sanjay M Sanlaville, Damien Cheung, Sau W Ernst, Carl Campeau, Philippe M Producer: 20190903 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay. [electronic resource] by Mucha, Bettina E Banka, Siddharth Ajeawung, Norbert Fonya Molidperee, Sirinart Chen, Gary G Koenig, Mary Kay Adejumo, Rhamat B Till, Marianne Harbord, Michael Perrier, Renee Lemyre, Emmanuelle Boucher, Renee-Myriam Skotko, Brian G Waxler, Jessica L Thomas, Mary Ann Hodge, Jennelle C Gecz, Jozef Nicholl, Jillian McGregor, Lesley Linden, Tobias Sisodiya, Sanjay M Sanlaville, Damien Cheung, Sau W Ernst, Carl Campeau, Philippe M Publication details: Genetics in medicine : official journal of the American College of Medical Genetics Sep 2019 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)