المؤلفون: Trzcionkowska, Kasia, Termote, Jacqueline U.M., van Genderen, Maria M., de Vries, Meindert J., van Sorge, Arlette J., Schalij-Delfos, Nicoline E.

المساهمون: MS Neonatologie, Child Health, MS Oogheelkunde

مصطلحات موضوعية: Concomitant disabilities, Guideline, Retinopathy of prematurity, Visual impairment, Pediatrics, Perinatology, and Child Health, Obstetrics and Gynaecology

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/449456

الاتاحة: https://dspace.library.uu.nl/handle/1874/449456

المؤلفون: Vercauteren, Leonie, Consejo, Alejandra, De Vries, Meindert Jan, Krolo, Iva, Koppen, Carina, Ní Dhubhghaill, Sorcha

المصدر: Eye & Contact Lens: Science & Clinical Practice; Jul2024, Vol. 50 Issue 7, p321-328, 8p

المؤلفون: MS Neonatologie, Child Health, MS Oogheelkunde, Trzcionkowska, Kasia, Termote, Jacqueline U.M., van Genderen, Maria M., de Vries, Meindert J., van Sorge, Arlette J., Schalij-Delfos, Nicoline E.

URL: https://doi.org/10.1016/j.earlhumdev.2023.105793
http://hdl.handle.net/1874/449456
http://www.scopus.com/inward/record.url?scp=85160331587&partnerID=8YFLogxK
0378-3782
Early Human Development
182
105793

المؤلفون: Bauwens, Miriam, Garanto, Alejandro, Sangermano, Riccardo, Naessens, Sarah, Weisschuh, Nicole, De Zaeytijd, Julie, Khan, Mubeen, Sadler, Françoise, Balikova, Irina, Van Cauwenbergh, Caroline, Rosseel, Toon, Bauwens, Jim, De Leeneer, Kim, De Jaegere, Sarah, Van Laethem, Thalia, De Vries, Meindert, Carss, Keren, Arno, Gavin, Fakin, Ana, Webster, Andrew R, de Ravel de l'Argentière, Thomy J L, Sznajer, Yves, Vuylsteke, Marnik, Kohl, Susanne, Wissinger, Bernd, Cherry, Timothy, Collin, Rob W J, Cremers, Frans P M, Leroy, Bart P, De Baere, Elfride

المساهمون: UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Centre de génétique médicale UCL

المصدر: Genetics in medicine, Vol. 21, no.8, p. 1761-1771 (2019)

مصطلحات موضوعية: ATP-Binding Cassette Transporters, Adult, Alleles, Cohort Studies, Exons, Female, Gene Frequency, Genes, Recessive, HEK293 Cells, Humans, Introns, Male, Middle Aged, Mutation, Oligonucleotides, Antisense, Pedigree, Phenotype, Retinal Dystrophies, ABCA4-associated disease, AON, Deep-intronic, Missing heritability, Noncoding

Relation: boreal:244295; http://hdl.handle.net/2078.1/244295; info:pmid/30670881; urn:ISSN:1098-3600; urn:EISSN:1530-0366

الاتاحة: http://hdl.handle.net/2078.1/244295
https://doi.org/10.1038/s41436-018-0420-y

المؤلفون: Verdin, Hannah, Rosseel, Toon, Vermeer, Sascha, Balikova, Irina, Kestelyn, Philippe, Meunier, Colombine, Meire, Françoise, Van De Velde, Julie, Vanakker, Olivier, Van Den Ende, Jenneke, De Rademaeker, Marjan, Meuwissen, Marije, De Vries, Meindert Jan, Sznajer, Yves, Desmet, Matthias, Sante, Tom, Coppieters, Frauke, Leroy, Bart, De Baere, Elfride

المصدر: Belgian Society for Human Genetics, 20th Annual meeting, Abstracts

مصطلحات موضوعية: Medicine and Health Sciences

Relation: https://biblio.ugent.be/publication/8655945

الاتاحة: https://biblio.ugent.be/publication/8655945
http://hdl.handle.net/1854/LU-8655945

المؤلفون: Geldof, Christiaan JA, Oosterlaan, Jaap, Vuijk, Pieter Jelle, de Vries, Meindert J, Kok, Joke H, van Wassenaer‐Leemhuis, Aleid G

المساهمون: Novum Foundation

المصدر: Developmental Medicine & Child Neurology ; volume 56, issue 9, page 862-868 ; ISSN 0012-1622 1469-8749

الاتاحة: http://dx.doi.org/10.1111/dmcn.12404
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fdmcn.12404
https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.12404

المؤلفون: Dik, Marjolein, de Vries, Meindert, Verbunt, Hélène, Lijnders, Henriette, van der Steen, Sanny

المصدر: Strabismus ; volume 20, issue 2, page 43-43 ; ISSN 0927-3972 1744-5132

الاتاحة: http://dx.doi.org/10.3109/09273972.2012.680237
http://www.tandfonline.com/doi/pdf/10.3109/09273972.2012.680237

المؤلفون: Weisschuh, Nicole, Stingl, Katarina, Audo, Isabelle, Biskup, Saskia, Bocquet, Beatrice, Branham, Kari, Burstedt, Marie, De Baere, Elfride, De Vries, Meindert J., Golovleva, Irina, Green, Andrew, Heckenlively, John, Leroy, Bart P., Meunier, Isabelle, Traboulsi, Elias, Wissinger, Bernd, Kohl, Susanne

المصدر: Human Mutation. 39(10):1366-1371

مصطلحات موضوعية: achromatopsia, cone phosphodiesterase, mutation spectrum and prevalence, PDE6C

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-152387

المؤلفون: UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Centre de génétique médicale UCL, Bauwens, Miriam, Garanto, Alejandro, Sangermano, Riccardo, Naessens, Sarah, Weisschuh, Nicole, De Zaeytijd, Julie, Khan, Mubeen, Sadler, Françoise, Balikova, Irina, Van Cauwenbergh, Caroline, Rosseel, Toon, Bauwens, Jim, De Leeneer, Kim, De Jaegere, Sarah, Van Laethem, Thalia, De Vries, Meindert, Carss, Keren, Arno, Gavin, Fakin, Ana, Webster, Andrew R, de Ravel de l'Argentière, Thomy J L, Sznajer, Yves, Vuylsteke, Marnik, Kohl, Susanne, Wissinger, Bernd, Cherry, Timothy, Collin, Rob W J, Cremers, Frans P M, Leroy, Bart P, De Baere, Elfride

المصدر: Genetics in medicine, Vol. 21, no.8, p. 1761-1771 (2019)

مصطلحات الفهرس: ATP-Binding Cassette Transporters, Adult, Alleles, Cohort Studies, Exons, Female, Gene Frequency, Genes, Recessive, HEK293 Cells, Humans, Introns, Male, Middle Aged, Mutation, Oligonucleotides, Antisense, Pedigree, Phenotype, Retinal Dystrophies, ABCA4-associated disease, AON, Deep-intronic, Missing heritability, Noncoding, info:eu-repo/semantics/article

URL: http://hdl.handle.net/2078.1/244295

المؤلفون: Geldof, Christiaan Ja, Oosterlaan, Jaap, Vuijk, Pieter Jelle, de Vries, Meindert J, Kok, Joke H, van Wassenaer-Leemhuis, Aleid G

المصدر: Developmental Medicine & Child Neurology; Apr2013, Vol. 55 Issue 4, p862-868, 7p

المؤلفون: de Vries, Meindert J, Yakimoff, Naum, Spekreijse, Henk

المصدر: Perception ; volume 18, issue 5, page 615-625 ; ISSN 0301-0066 1468-4233

الاتاحة: http://dx.doi.org/10.1068/p180615
http://journals.sagepub.com/doi/pdf/10.1068/p180615

المؤلفون: De Vries, Meindert, Van Dijk, Bob, Spekreijse, Henk

المصدر: Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section ; volume 74, issue 2, page 81-87 ; ISSN 0168-5597

الاتاحة: http://dx.doi.org/10.1016/0168-5597(89)90012-9
https://api.elsevier.com/content/article/PII:0168559789900129?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:0168559789900129?httpAccept=text/plain