يعرض 1 - 10 نتائج من 3,531 نتيجة بحث عن '"school child"', وقت الاستعلام: 1.86s تنقيح النتائج
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    دورية أكاديمية
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    دورية أكاديمية

    المصدر: Revista Ibero-Americana de Humanidades, Ciências e Educação; Vol. 10 No. 1 (2024): Revista Ibero-Americana de Humanidades, Ciências e Educação- REASE ; 84-97 ; Revista Ibero-Americana de Humanidades, Ciências e Educação; v. 10 n. 1 (2024): Revista Ibero-Americana de Humanidades, Ciências e Educação- REASE ; 2675-3375 ; 10.51891/rease.v10i1

    وصف الملف: application/pdf

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    دورية أكاديمية

    المؤلفون: Lina Lago

    المصدر: Confero: Essays on Education, Philosophy and Politics, Vol 9, Iss 2 (2023)

    وصف الملف: electronic resource

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    دورية أكاديمية
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    المصدر: Journal of Human Genetics. 66(10):995-1008

    مصطلحات موضوعية: c2cd3 protein, complementary DNA, dync2h1 protein, evc protein, evc2 protein, genomic DNA, ift74 protein, kiaa0753 protein, protein, ttc21b protein, unclassified drug, wdr19 protein, C2cd3 protein, human, cytoplasmic dynein, cytoskeleton protein, DYNC2H1 protein, EVC protein, EVC2 protein, isoprotein, KIAA0753 protein, membrane protein, microtubule associated protein, signal peptide, TTC21B protein, WDR19 protein, adolescent, adult, amino terminal sequence, Article, asphyxiating thoracic dystrophy, blood sampling, child, chondrodysplasia, chromosome 1q, chromosome 1q24q25, ciliopathy, clinical article, clinical feature, cohort analysis, comparative genomic hybridization, computer model, controlled study, copy number variation, cranioectodermal dysplasia, developmental delay, diagnostic value, DNA extraction, DNA sequencing, DNA splicing, Ellis van Creveld syndrome, exon, female, fetus, fetus lung, gene deletion, gene expression, gene sequence, genetic screening, human tissue, infant, Joubert syndrome, lung parenchyma, male, molecular diagnosis, nephronophthisis, newborn, pedigree, phenotype, preschool child, retrospective study, RNA analysis, school child, short rib polydactyly syndrome type 3, single nucleotide polymorphism, skeleton malformation, transcription initiation site, whole exome sequencing, whole genome sequencing, aged, bone dysplasia, genetic predisposition, genetics, high throughput sequencing, human genome, metabolism, middle aged, pathology, skeletal muscle, Bone Diseases, Developmental, Ciliopathies, Cytoplasmic Dyneins, Cytoskeletal Proteins, Genetic Predisposition to Disease, Genome, Human, High-Throughput Nucleotide Sequencing, Humans, Intercellular Signaling Peptides and Proteins, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Microtubule-Associated Proteins, Muscle, Skeletal, Protein Isoforms

    وصف الملف: print