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Weegerink, Nicole J.D.
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1

Phenotype of a Belgian Family With 6p25 Deletion Syndrome:

Weegerink, Nicole J.D. ; Swinnen, Freya K.R. ; Vanakker, Olivier M...
Annals of Otology, Rhinology & Laryngology.  125 (2016)  9 - p. 734-745 , 2016
Link: https://doi.org/10.1177/..
 
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2

Phenotypes of Two Dutch DFNA3 Families with Mutations in GJ..:

Weegerink, Nicole J. D. ; Pennings, Ronald J. E. ; Huygen, Patrick L. M....
Annals of Otology, Rhinology & Laryngology.  120 (2011)  3 - p. 191-197 , 2011
Link: https://doi.org/10.1177/..
 
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3

Genotype–Phenotype Correlation in DFNB8/10 Families with TM..:

Weegerink, Nicole J. D. ; Schraders, Margit ; Oostrik, Jaap...
Journal of the Association for Research in Otolaryngology.  12 (2011)  6 - p. 753-766 , 2011
Link: https://doi.org/10.1007/..
 
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4

Phenotype of the first otosclerosis family linked to OTSC10:

Weegerink, Nicole J.D. ; Schrauwen, Isabelle ; Huygen, Patrick L.M....
The Laryngoscope.  121 (2011)  4 - p. 838-845 , 2011
Link: https://doi.org/10.1002/..
 
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5

Genotype–Phenotype Correlation in DFNB8/10 Families with TM..:

Weegerink, Nicole J. D ; Schraders, Margit ; Oostrik, Jaap...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214237.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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6

Next-Generation Sequencing Identifies Mutations of SMPX, wh..:

Schraders, Margit ; Haas, Stefan A ; Weegerink, Nicole J.D...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146715.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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