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المؤلفون: Thomas, Eggermann, Florian, Kraft, Katja, Kloth, Eva, Klopocki, Irina, Hüning, Maja, Hempel, Erdmute, Kunstmann
المصدر: Clinical geneticsREFERENCES. 98(4)
مصطلحات موضوعية: Male, Beckwith-Wiedemann Syndrome, Chromosomes, Human, Pair 11, Infant, Newborn, Infant, Genomic Imprinting, Silver-Russell Syndrome, Phenotype, Insulin-Like Growth Factor II, Child, Preschool, Chromosome Duplication, Humans, Female, Genetic Predisposition to Disease, RNA, Long Noncoding, Chromosome Deletion, Child, Alleles
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::845014599d70be096827dd18748f2e70Test
https://pubmed.ncbi.nlm.nih.gov/33294970Test -
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المؤلفون: Stephen R F, Twigg, Deborah, Lloyd, Dagan, Jenkins, Nursel E, Elçioglu, Christopher D O, Cooper, Nouriya, Al-Sannaa, Ali, Annagür, Gabriele, Gillessen-Kaesbach, Irina, Hüning, Samantha J L, Knight, Judith A, Goodship, Bernard D, Keavney, Philip L, Beales, Opher, Gileadi, Simon J, McGowan, Andrew O M, Wilkie
المصدر: American journal of human genetics. 91(5)
مصطلحات موضوعية: Male, Genotype, Facies, Membrane Proteins, Acrocephalosyndactylia, Animals, Genetically Modified, Child, Preschool, Report, Mutation, Animals, Humans, Female, Child, Alleles, Genetic Association Studies, Zebrafish
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::8b9e996527f782c0f2030b2928de1d1eTest
https://pubmed.ncbi.nlm.nih.gov/23063620Test