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Feenstra, I.
434
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Online (434)
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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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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/..
?
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..
1-15