المؤلفون: Meire, F. M., Candaele, C., Van Coster, R., Cochaux, P., Obermaier-Kusser, B., Martin, J.-J.

المصدر: Ophthalmic Genetics ; volume 16, issue 3, page 119-126 ; ISSN 1381-6810 1744-5094

الإتاحة: https://doi.org/10.3109/13816819509059971Test

المؤلفون: Dal Cin, Paola, Sciot, Raphael, Speleman, F, Samson, Ignace, Laureys, G, de Potter, C, Meire, F, Van Damme, Boudewijn, Van den Berghe, Herman

مصطلحات موضوعية: Adult, Child, Chromosome Aberrations, Chromosomes, Human, Pair 11, Pair 2, Pair 6, Female, Fibrous Dysplasia of Bone, Humans, Karyotyping

العلاقة: Cancer Genetics and Cytogenetics vol:77 issue:2 pages:114-7; https://lirias.kuleuven.be/handle/123456789/28047Test

الإتاحة: https://lirias.kuleuven.be/handle/123456789/28047Test

المؤلفون: Meire, F M, Fryns, Jean-Pierre

مصطلحات موضوعية: Chromosomes, Human, Pair 21, Humans, Infant, Newborn, Lens Subluxation, Male, Mosaicism, Optic Nerve, Ring Chromosomes

العلاقة: Annales de Génétique vol:37 issue:3 pages:150-2; https://lirias.kuleuven.be/handle/123456789/276018Test

الإتاحة: https://lirias.kuleuven.be/handle/123456789/276018Test

المؤلفون: Buys, K, Casteels, Ingele, Vianna, R, Dralands, Godelieve, Leys, Anita, Meire, F, Missotten, Luc

مصطلحات موضوعية: Adolescent, Adult, Child, Preschool, Chorioretinitis, Cicatrix, Humans, Long-Term Care, Toxoplasmosis, Ocular, Visual Acuity

العلاقة: Bulletin de la Société belge d'ophtalmologie vol:248 pages:59; https://lirias.kuleuven.be/handle/123456789/18136Test

الإتاحة: https://lirias.kuleuven.be/handle/123456789/18136Test

المؤلفون: Bergen, A. A. B., Meire, F., Schuurman, E. J. M., Delleman, J. W.

المصدر: Clinical Genetics ; volume 45, issue 5, page 236-240 ; ISSN 0009-9163 1399-0004

الإتاحة: https://doi.org/10.1111/j.1399-0004.1994.tb04148.xTest

المؤلفون: Arthur Bergen, Ten Brink, J., Riemslag, F., Soest, S., Schuurman, E., Meire, F., Tijmes, N., Jong, P. T. V. M.

المساهمون: Human Genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Ophthalmology

المصدر: Investigative Ophthalmology and Visual Science, 37(3). Association for Research in Vision and Ophthalmology Inc.
Scopus-Elsevier

مصطلحات موضوعية: eye diseases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::127b22b44ed8ae5b44df548305966661Test
https://pure.amc.nl/en/publications/are-xlinked-congenital-stationary-night-blindness-and-xlinked-retinitis-pigmentosa-genetically-allelicTest(e1e8d882-59bb-4d8c-8215-0fd18ffdfb78).html

المؤلفون: Verloes, Alain, Journel, H., Elmer, C., Misson, Jean-Paul, Le Merrer, M., Kaplan, J., Van Maldergem, Lionel, Deconinck, H., Meire, F.

المصدر: American Journal of Medical Genetics, 46(2), 132-137. (1993).

مصطلحات موضوعية: megalocornea heterogeneity, Neuhauser syndrome, iris hypoplasia, macrocephaly, Human health sciences :: Neurology, Sciences de la santé humaine :: Neurologie, Human health sciences :: Pediatrics, Sciences de la santé humaine :: Pédiatrie, art, psy

العلاقة: https://orbi.uliege.be/handle/2268/63842Test

الإتاحة: https://orbi.uliege.be/handle/2268/63842Test

المؤلفون: Meire, F. M., Delleman, J. W.

المصدر: Ophthalmic Paediatrics and Genetics ; volume 13, issue 2, page 123-129 ; ISSN 0167-6784

الإتاحة: https://doi.org/10.3109/13816819209087612Test

المؤلفون: Obermaier-Kusser B, Lorenz B, Schubring S, Paprotta A, Zerres K, Thomas Meitinger, Meire F, Cochaux P, Blankenagel A, Kommerell G

المصدر: Europe PubMed Central

مصطلحات موضوعية: Male, Letter, Belgium, Optic Atrophies, Hereditary, Germany, Mutation, Humans, Female, DNA Probes, DNA, Mitochondrial, Pedigree

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::73c5383ba29117f9892b0d4df009185bTest
https://pubmed.ncbi.nlm.nih.gov/7977345Test

المؤلفون: Bergen, A. A., Meire, F., Schuurman, E. J., Delleman, J. W.

المساهمون: Other departments

المصدر: Clinical genetics, 45(5), 236-240. Wiley-Blackwell

مصطلحات موضوعية: genetic structures, sense organs, eye diseases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=narcis______::ded3e70c1ff4a86a3a32590172c88845Test
https://pure.amc.nl/en/publications/dna-carrier-detection-in-xlinked-progressive-cone-dystrophyTest(c67c844f-70db-4aac-a712-5289285a0766).html