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المصدر: Folia Medica, Vol 63, Iss 1, Pp 138-141 (2021)
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Intellectual development, Autism Spectrum Disorder, Epilepsy, 16p11.2 duplication, Gene Duplication, Intellectual Disability, Gene duplication, Intellectual disability, medicine, Humans, array CGH, Hypertelorism, Comparative Genomic Hybridization, autistic behavior, business.industry, Syndrome, General Medicine, medicine.disease, Pedigree, Phenotype, Molecular Diagnostic Techniques, Schizophrenia, Child, Preschool, Medicine, Female, medicine.symptom, Presentation (obstetrics), business, Chromosomes, Human, Pair 16, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a48da49a315ceeba1249df939221fa3Test
https://foliamedica.bg/article/52763/download/pdfTest/ -
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المؤلفون: Tingjuan Zhang, Jingdong Zhou, Yangli Zhao, Yangjing Zhao
المصدر: Cancer Biomarkers. 29:387-397
مصطلحات موضوعية: Male, Oncology, Cancer Research, medicine.medical_treatment, Datasets as Topic, Kaplan-Meier Estimate, Hematopoietic stem cell transplantation, Translocation, Genetic, chemistry.chemical_compound, 0302 clinical medicine, Bone Marrow, hemic and lymphatic diseases, Aged, 80 and over, 0303 health sciences, Gene Expression Regulation, Leukemic, Hematopoietic Stem Cell Transplantation, Myeloid leukemia, General Medicine, Middle Aged, Prognosis, RUNX2, Leukemia, Myeloid, Acute, RUNX1, 030220 oncology & carcinogenesis, Core Binding Factor Alpha 2 Subunit, Female, Chromosomes, Human, Pair 8, Adult, medicine.medical_specialty, Adolescent, Disease-Free Survival, Young Adult, 03 medical and health sciences, Internal medicine, Cancer genome, microRNA, Genetics, medicine, Humans, neoplasms, Transcription factor, Aged, 030304 developmental biology, Chemotherapy, business.industry, DNA Methylation, Core Binding Factor Alpha 3 Subunit, chemistry, Case-Control Studies, Mutation, Neoplasm Recurrence, Local, business, Chromosomes, Human, Pair 16
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e85a5f27a3e0598a801609486b5c23Test
https://doi.org/10.3233/cbm-200016Test -
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المؤلفون: Heyang Zhang, Qianru Zhan, Xiaoxue Wang, Feng Gao, Jinxiang Yu, Jing Wang, Wei Fu, Pingping Wang, Xin Wei, Lijun Zhang
المصدر: Annals of hematology. 101(12)
مصطلحات موضوعية: Male, Adult, Chromosomes, Human, Pair 21, Interleukin-3 Receptor alpha Subunit, Hematology, General Medicine, Middle Aged, Translocation, Genetic, Leukemia, Myeloid, Acute, Transcriptional Regulator ERG, Myelodysplastic Syndromes, Acute Disease, Humans, RNA-Binding Protein FUS, Female, Chromosomes, Human, Pair 16, Retrospective Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0621fab3d1d84525300c9cbd733faa1Test
https://pubmed.ncbi.nlm.nih.gov/36181538Test -
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المؤلفون: Guilin Tang, Ying Zou, Sa A. Wang, Gautam Borthakur, Gokce Toruner, Shimin Hu, Shaoying Li, Jie Xu, L. Jeffrey Medeiros, Zhenya Tang
المصدر: Annals of hematology. 101(4)
مصطلحات موضوعية: Leukemia, Myeloid, Acute, Oncogene Proteins, Fusion, Recurrence, Chromosome Inversion, Hematopoietic Stem Cell Transplantation, Humans, Hematology, General Medicine, Chromosomes, Human, Pair 16, Core Binding Factor beta Subunit, In Situ Hybridization, Fluorescence, Sequence Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef25a41f27bf2a32c6d980c5715dac1dTest
https://pubmed.ncbi.nlm.nih.gov/35184217Test -
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المؤلفون: Jing Liu, Baiyun Chen, Yuchun Liu, Jinghui Kong, Bo Zhang, Liang Han, Daoqi Mei, Cai Yun Ma, Qing Shang, Zhenhua Xie, Mengjun Xiao, Shiyue Mei, Yaodong Zhang, Chao Gao, Dongxiao Li
المصدر: European journal of medical genetics. 65(9)
مصطلحات موضوعية: Developmental Disabilities, Intellectual Disability, Homozygote, Genetics, Humans, General Medicine, Uniparental Disomy, Genetics (clinical), Chromosomes, Human, Pair 16, Transaminases
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e38846643309ab9fa735866a764aed4Test
https://pubmed.ncbi.nlm.nih.gov/35793769Test -
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المؤلفون: Guillermo Garcia-Manero, Endi Wang, Hagop M. Kantarjian, Shimin Hu, Carlos E. Bueso-Ramos, Young L. Kim, Qi Shen, Yi Zhou, Sanam Loghavi, L. Jeffrey Medeiros, Sa Wang, Wei Xie, Aileen Y. Hu, Guiling Tang, Adam Cloe
المصدر: Annals of Hematology. 99:487-500
مصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, Databases, Factual, Oncogene Proteins, Fusion, Malignancy, Risk Assessment, Translocation, Genetic, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Humans, Topoisomerase II Inhibitors, Cytotoxic T cell, Neoplasm, Pathological, Aged, Aged, 80 and over, Hematology, biology, business.industry, Chromosomes, Human, Pair 11, Myeloid leukemia, Neoplasms, Second Primary, Histone-Lysine N-Methyltransferase, General Medicine, Middle Aged, medicine.disease, CREB-Binding Protein, Leukemia, Myeloid, Acute, KMT2A, Dysplasia, Hematologic Neoplasms, Myelodysplastic Syndromes, 030220 oncology & carcinogenesis, biology.protein, Female, business, Chromosomes, Human, Pair 16, Myeloid-Lymphoid Leukemia Protein, 030215 immunology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35323f8db4c2f5ebab8914b85eb23407Test
https://doi.org/10.1007/s00277-020-03909-7Test -
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المؤلفون: F Simone, C. Liccese, R. Davanzo, C. Dilucca, Maria Giovanna Lupo, Domenico Dell’Edera, Arianna Allegretti
المصدر: Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-6 (2018)
Journal of Medical Case Reportsمصطلحات موضوعية: Male, Parents, 0301 basic medicine, Proband, Developmental delay, Developmental Disabilities, Submicroscopic chromosomal changes, Intellectual disability, lcsh:Medicine, Case Report, Chromosome Disorders, 030105 genetics & heredity, Child, In Situ Hybridization, In Situ Hybridization, Fluorescence, media_common, Genetics, CGH-array, Daughter, medicine.diagnostic_test, General Medicine, Microdeletion syndrome, Phenotype, 16p11.2 microdeletion syndrome, Autism spectrum disorder, Child, Preschool, Female, Chromosome Deletion, Abnormality, Human, Adult, media_common.quotation_subject, Chromosomes, Fluorescence, 03 medical and health sciences, Thinness, medicine, Humans, Autistic Disorder, Preschool, Pair 16, business.industry, lcsh:R, medicine.disease, Etiology, business, Chromosomes, Human, Pair 16, Intellectual Disability, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00a884a074fe3d460702ee6283dc900eTest
http://link.springer.com/article/10.1186/s13256-018-1587-1Test -
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المؤلفون: Susanne Kohl, Ieva Sliesoraityte, Laura Kühlewein, Mary J. van Schooneveld, Bernd Wissinger, Eberhart Zrenner, Alexandra Sauer, Günther Rudolph, Pablo Llavona, Melanie Kempf, Florian A. Dehmelt, Peggy Reuter, Aristides B. Arrenberg, Nicole Weisschuh
المصدر: Human Molecular Genetics
مصطلحات موضوعية: 0301 basic medicine, Male, AcademicSubjects/SCI01140, genetic structures, Color vision, Locus (genetics), Color Vision Defects, 03 medical and health sciences, 0302 clinical medicine, Cone dystrophy, Gene duplication, Gene cluster, Chromosome Duplication, Genetics, medicine, Animals, Humans, Cone Dystrophy, Molecular Biology, Zebrafish, Genetics (clinical), Genes, Dominant, Family Health, Homeodomain Proteins, Comparative Genomic Hybridization, biology, General Medicine, Sequence Analysis, DNA, medicine.disease, biology.organism_classification, eye diseases, Pedigree, 030104 developmental biology, Gene Expression Regulation, Multigene Family, 030221 ophthalmology & optometry, Female, General Article, Retinal Dystrophies, Chromosomes, Human, Pair 16, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2256018fbbd522bbeac2b99dd0facd4eTest
https://pubmed.ncbi.nlm.nih.gov/33891002Test -
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المؤلفون: Kamran Guity, Maryam S. Daneshpour, Fereidoun Azizi, Farid Zayeri, Yadollah Mehrabi, Nima Hosseinzadeh
المصدر: Gene. 692:156-169
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Single-nucleotide polymorphism, Iran, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, 03 medical and health sciences, 0302 clinical medicine, Chromosome 16, Pleiotropy, Plasma lipids, Genetics, Humans, SNP, Solute Carrier Family 12, Member 3, Gene, Triglycerides, Genetic association, Cholesterol, HDL, Intracellular Signaling Peptides and Proteins, RNA-Binding Proteins, Genetic Pleiotropy, General Medicine, Middle Aged, Lipids, Cholesterol Ester Transfer Proteins, Pedigree, 030104 developmental biology, 030220 oncology & carcinogenesis, Female, Family based, Chromosomes, Human, Pair 16, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf12aafba76e73c6fb446a06436025f8Test
https://doi.org/10.1016/j.gene.2019.01.007Test -
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المؤلفون: Caiqun Luo, Niping Jiang, Mei Zhong, Jiansheng Xie, Shengli Li, Guanglin Zhang, Yang Liu, Hui Wang
المصدر: Fetal and Pediatric Pathology. 37:452-464
مصطلحات موضوعية: 0301 basic medicine, Placenta, Intrauterine growth restriction, 030105 genetics & heredity, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Chromosome 16, Pregnancy, medicine, Humans, Clinical significance, Genetics, Fetus, Fetal Growth Retardation, 030219 obstetrics & reproductive medicine, Microarray analysis techniques, business.industry, Chromosome, General Medicine, Uniparental Disomy, medicine.disease, Uniparental disomy, Pediatrics, Perinatology and Child Health, Female, business, Chromosomes, Human, Pair 16
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad7206155062b49935efed4d03f84104Test
https://doi.org/10.1080/15513815.2018.1538275Test