المؤلفون: LM Dibbens, S Mullen, I Helbig, HC Mefford, MA Bayly, S Bellows, C Leu, H Trucks, T Obermeier, M Wittig, A Franke, H Caglayan, Z Yapici, T Sander, EE Eichler, IE Scheffer, JC Mulley, SF Berkovic, P De Jonghe, A Suls, H Hjalgrim, JM Madsen, RS Møller, AE Lehesjoki, A Siren, V Gaus, D Janz, B Schmitz, CE Elger, K Hallmann, AA Kleefuß-Lie, WS Kunz, A Raabe, H Muhle, P Ostertag, S von Spiczak, U Stephani, H Lerche, YG Weber, P Striano, F Zara, C Marini, EH Brilstra, D Kastelijn-Nolst Trenité, BPC Koeleman, CGF de Kovel, D Lindhout, MEM Swinkels, O Yalcin, B Baykan, D Turkdogan, G Dizdarer, C Ozkara, Y Lee, J Müller-Quernheim, R Fölster-Holst, S Hofmann, A Nebel, S Schreiber, M Schürmann, E Rodriguez, S Weidinger, H Baurecht, BA Lie, KM Boberg, TH Karlsen

مصطلحات موضوعية: Uncategorised value

Relation: http://hdl.handle.net/10536/DRO/DU:30111755; https://figshare.com/articles/journal_contribution/Familial_and_sporadic_15q13_3_microdeletions_in_idiopathic_generalized_epilepsy_precedent_for_disorders_with_complex_inheritance/20804398

الاتاحة: http://hdl.handle.net/10536/DRO/DU:30111755
https://figshare.com/articles/journal_contribution/Familial_and_sporadic_15q13_3_microdeletions_in_idiopathic_generalized_epilepsy_precedent_for_disorders_with_complex_inheritance/20804398

المؤلفون: Ng, Laing, Bt, Majda, P Anthony Akkari, Mg, Layton, Jc, Mulley, Phillips H, Ea, Haan, Sj, White, Ah, Beggs, Lm, Kunkel

المصدر: P Anthony Akkari

مصطلحات موضوعية: Chromosome Aberrations, Male, Genetic Linkage, Chromosome Mapping, Chromosome Disorders, Neuromuscular Diseases, Original Articles, DNA, Satellite, Chromosomes, Human, Pair 1, Child, Preschool, Humans, Actinin, Female, Lod Score, Child, Polymorphism, Restriction Fragment Length, Genes, Dominant

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8a54219093b1752065272fc26f913397
https://pubmed.ncbi.nlm.nih.gov/1347195

المؤلفون: Ri, Richards, Shen Y, Holman K, Kozman H, Valentine Hyland, Jc, Mulley, Gr, Sutherland

المصدر: Europe PubMed Central

مصطلحات موضوعية: Genetic Markers, congenital, hereditary, and neonatal diseases and abnormalities, Polymorphism, Genetic, Base Sequence, Genetic Linkage, Molecular Sequence Data, DNA, DNA, Satellite, Pedigree, Fragile X Syndrome, Autoradiography, Humans, Lod Score, Alleles, Repetitive Sequences, Nucleic Acid, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::297e3050faff3098af7947863ed24826
https://pubmed.ncbi.nlm.nih.gov/2035525

المؤلفون: Jc, Mulley, Hm, Kozman, Ha, Phillips, Ak, Gedeon, Ja, Mccure, Iles DE, Ronald Gregg, Hogan K, Fj, Couch, Dh, Maclennan

المصدر: Europe PubMed Central

مصطلحات موضوعية: Male, Recombination, Genetic, Genetic Linkage, Chromosome Mapping, macromolecular substances, Original Articles, musculoskeletal system, Pedigree, Meiosis, Phenotype, Muscular Diseases, Humans, Female, Child, Malignant Hyperthermia, tissues, Chromosomes, Human, Pair 19, Alleles, Genes, Dominant

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ea77e58f691347fe0b3ab7ec139d3552
http://europepmc.org/abstract/med/8430700

المؤلفون: KD Shearer, JC Mulley

المصدر: Marine and Freshwater Research. 29:551

مصطلحات موضوعية: education.field_of_study, Ecology, Population, Zoology, Aquatic Science, Biology, Oceanography, biology.organism_classification, Cyprinus, Fishery, Phylogeography, Carassius auratus, Fish , Carp, education, Mollusca, Ecology, Evolution, Behavior and Systematics, Invertebrate

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::158c32b3a4353d6b31707fa925df1a13
https://doi.org/10.1071/mf9780551

المؤلفون: JC Mulley, KD Shearer

المصدر: Marine and Freshwater Research. 31:409

مصطلحات موضوعية: Ecology, biology, Aquatic Science, Oceanography, biology.organism_classification, Cyprinus, Phylogeography, Fish , Identification (biology), Carp, Ecology, Evolution, Behavior and Systematics, Hybrid, Invertebrate

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a49b98e2092418878b6a893aac4e05c5
https://doi.org/10.1071/mf9800409