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Feenstra, I.
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1

Stable long-term outcomes after cochlear implantation in su..:

Fehrmann, M. L. A. ; Huinck, W. J. ; Thijssen, M. E. G....
Journal of Otolaryngology - Head & Neck Surgery.  52 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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2

Correction to: Exploring the missing heritability in subjec..:

Smits, Jeroen J. ; de Bruijn, Suzanne E. ; Lanting, Cornelis P....
Human Genetics.  , 2021
Link: https://doi.org/10.1007/..
 
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3

Exploring the missing heritability in subjects with hearing..:

Smits, Jeroen J. ; de Bruijn, Suzanne E. ; Lanting, Cornelis P....
Human Genetics.  141 (2021)  3-4 - p. 465-484 , 2021
Link: https://doi.org/10.1007/..
 
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4

Further audiovestibular characterization of DFNB77, caused ..:

Wesdorp, M. ; Schreur, V. ; Beynon, A.J....
Clinical Genetics.  94 (2018)  2 - p. 221-231 , 2018
Link: https://doi.org/10.1111/..
 
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5

Clinical utility of non‐invasive prenatal testing in pregna..:

Beulen, L. ; Faas, B. H. W. ; Feenstra, I...
Ultrasound in Obstetrics & Gynecology.  49 (2017)  6 - p. 721-728 , 2017
Link: https://doi.org/10.1002/..
 
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6

Genotype phenotype correlations for hearing impairment: App..:

Hoefsloot, L. H. ; Feenstra, I. ; Kunst, H. P. M..
Clinical Genetics.  85 (2014)  6 - p. 514-523 , 2014
Link: https://doi.org/10.1111/..
 
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7

Patient experiences with gene panels based on exome sequenc..:

Sie, A.S. ; Prins, J.B. ; van Zelst-Stams, W.A.G....
Clinical Genetics.  87 (2014)  4 - p. 319-326 , 2014
Link: https://doi.org/10.1111/..
 
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8

Novel BCOR mutations in patients with oculofaciocardiodenta..:

Feberwee, H.E. ; Feenstra, I. ; Oberoi, S....
Clinical Genetics.  85 (2013)  2 - p. 194-197 , 2013
Link: https://doi.org/10.1111/..
 
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9

P-711 - Genetic syndromes and the autism spectrum:

Verhoeven, W.M.A. ; Egger, J.I.M. ; Feenstra, I.
European Psychiatry.  27 (2012)  - p. 1 , 2012
Link: https://doi.org/10.1016/..
 
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10

W01-01 - From karyotype to targeted microarray:

Feenstra, I. ; Van Bon, B.W. ; Koolen, D.A....
European Psychiatry.  27 (2012)  - p. 1 , 2012
Link: https://doi.org/10.1016/..
 
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11

P-713 - A de novo microdeletion in chromosome 8q12.3q13.2: ..:

Verhoeven, W.M.A. ; Egger, J.I.M. ; Feenstra, I..
European Psychiatry.  27 (2012)  - p. 1 , 2012
Link: https://doi.org/10.1016/..
 
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12

Cryptic duplication of the distal segment of 22q due to a t..:

Feenstra, I. ; Koolen, D.A. ; Van der Pas, J....
European Journal of Medical Genetics.  49 (2006)  5 - p. 384-395 , 2006
Link: https://doi.org/10.1016/..
 
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13

European Cytogeneticists Association Register of Unbalanced..:

Feenstra, I. ; Fang, J. ; Koolen, D.A....
European Journal of Medical Genetics.  49 (2006)  4 - p. 279-291 , 2006
Link: https://doi.org/10.1016/..
 
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14

Globozoospermia revisited:

Dam, A.H.D.M. ; Feenstra, I. ; Westphal, J.R....
Human Reproduction Update.  13 (2006)  1 - p. 63-75 , 2006
Link: https://doi.org/10.1093/..
 
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15

All-in-one whole exome sequencing strategy with simultaneou..:

Faas, B.H.W ; Westra, D ; de Munnik, S.A...
https://cris.maastrichtuniversity.nl/en/publications/e53dca14-cf76-465a-8bb5-37513f149f4f.  , 2023
Link: https://cris.maastrichtu..
 
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