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The Annals of Otology, Rhinology, and Laryngology|June 1, 2016
Phenotype of a Belgian Family With 6p25 Deletion SyndromeNicole J D Weegerink, Freya K R Swinnen, Olivier M Vanakker, et al.The Annals of Otology, Rhinology, and Laryngology|April 23, 2011
Phenotypes of two Dutch DFNA3 families with mutations in GJB2Nicole J D Weegerink, Ronald J E Pennings, Patrick L M Huygen, et al.The Laryngoscope|March 25, 2011
Phenotype of the first otosclerosis family linked to OTSC10Nicole J D Weegerink, Isabelle Schrauwen, Patrick L M Huygen, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.American Journal of Human Genetics|May 10, 2011
Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairmentMargit Schraders, Stefan A Haas, Nicole J D Weegerink, et al.Journal of the Association for Research in Otolaryngology : JARO|July 26, 2011
Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutationsNicole J D Weegerink, Margit Schraders, Jaap Oostrik, et al.Pageof 1