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Genetics in Medicine, ISSN 1098-3600, 2019, Volume 21, Issue 5, pp. 1199 - 1208
Purpose: To characterize new molecular factors implicated in a hereditary congenital facial paresis (HCFP) family and otosclerosis. Methods: We performed exome... 
hereditary congenital facial paresis | MEPE | otosclerosis | hearing loss | craniofacial bone disorder | ETIOLOGY | EXTRACELLULAR PHOSPHOGLYCOPROTEIN MEPE | MOBIUS-SYNDROME | FAMILY | PEPTIDES | GENE | CONGENITAL FACIAL PALSY | MUTATION | GENETICS & HEREDITY | MOLECULAR INVERSION PROBES | EXPRESSION
Journal Article
CELL CYCLE, ISSN 1538-4101, 06/2010, Volume 9, Issue 11, pp. 2061 - 2062
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 07/2011, Volume 26, Issue 7, pp. 1425 - 1436
Journal Article