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1دورية أكاديمية
المؤلفون: Gergely Büki, Anna Zsigmond, Márta Czakó, Renáta Szalai, Gréta Antal, Viktor Farkas, György Fekete, Dóra Nagy, Márta Széll, Marianna Tihanyi, Béla Melegh, Kinga Hadzsiev, Judit Bene
المصدر: Frontiers in Genetics, Vol 12 (2021)
مصطلحات موضوعية: copy number variation, type-1 NF1 microdeletion, type-2 NF1 microdeletion, atypical NF1 microdeletion, 17q11.2 deletion syndrome, array-CGH, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fgene.2021.673025/fullTest; https://doaj.org/toc/1664-8021Test
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2
المؤلفون: Gergely Büki (5733695), Anna Zsigmond (10644164), Márta Czakó (5733698), Renáta Szalai (10939026), Gréta Antal (10939029), Viktor Farkas (1581013), György Fekete (8824568), Dóra Nagy (5893892), Márta Széll (177753), Marianna Tihanyi (10939032), Béla Melegh (177745), Kinga Hadzsiev (4406725), Judit Bene (725901)
مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, copy number variation, type-1 NF1 microdeletion, type-2 NF1 microdeletion, atypical NF1 microdeletion, 17q11.2 deletion syndrome, array-CGH, multiplex ligation-probe dependent amplification, NF1 gene
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3
المؤلفون: Gergely Büki, Anna Zsigmond, Márta Czakó, Renáta Szalai, Gréta Antal, Viktor Farkas, György Fekete, Dóra Nagy, Márta Széll, Marianna Tihanyi, Béla Melegh, Kinga Hadzsiev, Judit Bene
مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, copy number variation, type-1 NF1 microdeletion, type-2 NF1 microdeletion, atypical NF1 microdeletion, 17q11.2 deletion syndrome, array-CGH, multiplex ligation-probe dependent amplification, NF1 gene
الإتاحة: https://doi.org/10.3389/fgene.2021.673025.s003Test
https://figshare.com/articles/dataset/Table_3_Genotype-Phenotype_Associations_in_Patients_With_Type-1_Type-2_and_Atypical_NF1_Microdeletions_docx/14747469Test