id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_a3teo4nkrjcb7ffbyaeqibtfh4	Dan Doherty	GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome	2012	6	.pdf	application/pdf	4290	516	60	Autosomal-recessive inheritance, severe to profound sensorineural hearing loss, and partial agenesis of the corpus callosum are hallmarks of the clinically well-established Chudley-McCullough syndrome (CMS). Please cite this article in press as: Doherty et al., GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Please cite this article in press as: Doherty et al., GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Please cite this article in press as: Doherty et al., GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Please cite this article in press as: Doherty et al., GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Please cite this article in press as: Doherty et al., GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome	./cache/work_a3teo4nkrjcb7ffbyaeqibtfh4.pdf	./txt/work_a3teo4nkrjcb7ffbyaeqibtfh4.txt