المؤلفون: Beysen, D., Raes, J., Leroy, B.P., Lucassen, A., Yates, J.R.W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J.P., Kim, J.R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L.M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R.A., De Paepe, A., De Baere, E.

المصدر: The American Journal of Human Genetics ; volume 77, issue 2, page 205-218 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1086/432083Test
https://api.elsevier.com/content/article/PII:S0002929707629115?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929707629115?httpAccept=text/plainTest

المؤلفون: Bergen, A A, ten Brink, J B, Riemslag, F, Schuurman, E J, Meire, F, Tijmes, N, de Jong, P T

المصدر: Journal of Medical Genetics ; volume 33, issue 10, page 869-872 ; ISSN 1468-6244

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1136/jmg.33.10.869Test

المؤلفون: Bergen, A A, Kestelyn, P, Leys, M, Meire, F

المصدر: Journal of Medical Genetics ; volume 31, issue 7, page 580-582 ; ISSN 1468-6244

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1136/jmg.31.7.580Test

المؤلفون: Van Camp, Guy, van Thienen, Marie-Noëlle, Handig, I., van Roy, B., Rao, V.S., Milunsky, A., Read, A.P., Baldwin, C.T., Farrer, L.A., Bonduelle, M., Standaert, L., Meire, F., Willems, P.J.

المصدر: Journal of medical genetics

مصطلحات موضوعية: Male, PAX3, Biology, Microphthalmia, Genetic Heterogeneity, Mice, Species Specificity, Genetics, medicine, Animals, Humans, Paired Box Transcription Factors, Waardenburg Syndrome, Hirschsprung Disease, PAX3 Transcription Factor, Gene, Genetics (clinical), Regulation of gene expression, Microphthalmia-Associated Transcription Factor, Chromosomes, Human, Pair 13, Receptors, Endothelin, Waardenburg syndrome, Genetic heterogeneity, Genes, Homeobox, Infant, Newborn, Chromosome Mapping, Gene Expression Regulation, Developmental, Chromosome, medicine.disease, Microphthalmia-associated transcription factor, Receptor, Endothelin B, Mice, Mutant Strains, DNA-Binding Proteins, Neural Crest, Female, Chromosomes, Human, Pair 3, Chromosome Deletion, Lod Score, Microsatellite Repeats, Transcription Factors, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ce0390ad8e2fab69c42444f1782ab1eTest
https://doi.org/10.1136/jmg.32.7.531Test

المؤلفون: Oehler, M., Schwinger, E., Meire, F. M., Szabo, P., Gal, A.

المصدر: Human Genetics ; volume 87, issue 2, page 241-241 ; ISSN 0340-6717 1432-1203

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1007/bf00204195Test