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Irina Balikova

Showing results (1-10 of 36) with videos related to

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Retinal Cases & Brief Reports|February 7, 2020
MULTIMODAL IMAGING IN HELLP-RELATED CHORIORETINOPATHYCamille Van Rysselberge, Irina Balikova, Lia Judice, et al.
European Journal of Medical Genetics|March 11, 2009
Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)Irina Balikova, Joris Robert Vermeesch, Jean-Pierre Fryns, et al.
Ophthalmic Genetics|May 6, 2021
Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findingsDorien Herijgers, Ellen Denayer, Irina Balikova, et al.
European Journal of Human Genetics : EJHG|May 19, 2011
The causality of de novo copy number variants is overestimatedJoris R Vermeesch, Irina Balikova, Connie Schrander-Stumpel, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
"Opitz C syndrome and pseudohypoaldosteronism" is caused by a chromosome 4q deletionThomy de Ravel, Irina Balikova, Jozef Van Driessche, et al.
American Journal of Medical Genetics. Part A|March 29, 2005
Acrofacial dysostosis type RodríguezBoyan Dimitrov, Irina Balikova, Nely Jekova, et al.
Case Reports in Ophthalmology|October 30, 2023
Unilateral Melanoma-Associated Retinopathy Case ReportReinout Peeters, Freya Peeters, Julie Jacob, et al.
European Journal of Medical Genetics|March 17, 2009
Another patient with a de novo deletion further delineates the 2q33.1 microdeletion syndromeThomy J de Ravel, Irina Balikova, Paul Thiry, et al.
Acta Ophthalmologica|May 22, 2015
Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11Irina Balikova, Anthony G Robson, Graham E Holder, et al.
European Journal of Medical Genetics|March 23, 2020
Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicismElise Pozza, Hannah Verdin, Hilde Deconinck, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Retinal Cases & Brief Reports|February 7, 2020
MULTIMODAL IMAGING IN HELLP-RELATED CHORIORETINOPATHYCamille Van Rysselberge, Irina Balikova, Lia Judice, et al.
European Journal of Medical Genetics|March 11, 2009
Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)Irina Balikova, Joris Robert Vermeesch, Jean-Pierre Fryns, et al.
Ophthalmic Genetics|May 6, 2021
Two siblings with Heimler syndrome caused by PEX1 variants: follow-up of ophthalmologic findingsDorien Herijgers, Ellen Denayer, Irina Balikova, et al.
European Journal of Human Genetics : EJHG|May 19, 2011
The causality of de novo copy number variants is overestimatedJoris R Vermeesch, Irina Balikova, Connie Schrander-Stumpel, et al.
American Journal of Medical Genetics. Part A|May 19, 2009
"Opitz C syndrome and pseudohypoaldosteronism" is caused by a chromosome 4q deletionThomy de Ravel, Irina Balikova, Jozef Van Driessche, et al.
American Journal of Medical Genetics. Part A|March 29, 2005
Acrofacial dysostosis type RodríguezBoyan Dimitrov, Irina Balikova, Nely Jekova, et al.
Case Reports in Ophthalmology|October 30, 2023
Unilateral Melanoma-Associated Retinopathy Case ReportReinout Peeters, Freya Peeters, Julie Jacob, et al.
European Journal of Medical Genetics|March 17, 2009
Another patient with a de novo deletion further delineates the 2q33.1 microdeletion syndromeThomy J de Ravel, Irina Balikova, Paul Thiry, et al.
Acta Ophthalmologica|May 22, 2015
Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11Irina Balikova, Anthony G Robson, Graham E Holder, et al.
European Journal of Medical Genetics|March 23, 2020
Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicismElise Pozza, Hannah Verdin, Hilde Deconinck, et al.
Pageof 4