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1
المؤلفون: Adam Janssen, Renfang Song, Tian-Jian Chen, Ihor V. Yosypiv
المصدر: Pediatric research. 91(3)
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Multicystic dysplastic kidney, BBS9, Kidney, 03 medical and health sciences, 0302 clinical medicine, 030225 pediatrics, Gene duplication, Female patient, medicine, Humans, Multicystic Dysplastic Kidney, Child, Bardet-Biedl Syndrome, Cystic kidney, Monosomy X, Comparative Genomic Hybridization, business.industry, medicine.disease, Dysplasia, Pediatrics, Perinatology and Child Health, Female, business, Carrier Proteins, 030217 neurology & neurosurgery, Comparative genomic hybridization
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2
المؤلفون: Tian Lei, Tian Jian Chen, Shuai Li Wei, Xu Liu
المصدر: Applied Mechanics and Materials. 437:914-917
مصطلحات موضوعية: Engineering drawing, Engineering, business.product_category, business.industry, Design elements and principles, General Medicine, Machine tool, Image (mathematics), Industrial design, Element (category theory), Kansei engineering, business, Design methods, Semantic differential method
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3
المؤلفون: Shuai Liu, Wen Tao, Tian Jian Chen, Yuan Sun, Wei Dai
المصدر: Advanced Materials Research. 645:267-271
مصطلحات موضوعية: Mathematical optimization, Computer science, General Engineering, A* search algorithm, Adaptive routing, law.invention, Private Network-to-Network Interface, Shortest Path Faster Algorithm, Link-state routing protocol, law, Shortest path problem, Suurballe's algorithm, K shortest path routing, Pathfinding, Algorithm, Dijkstra's algorithm, Yen's algorithm, Constrained Shortest Path First
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c6584cb3be721321335eef6b5415598e
https://doi.org/10.4028/www.scientific.net/amr.645.267 -
4
المؤلفون: Rosemarie Smith, Elizabeth McCracken, Barbara McGillivray, Tian Jian Chen, Cynthia J. Curry, Taosheng Huang, Yao Shan Fan, Jose E. Martinez, Judith A. Martin, Diane Masser-Frye, Hongbo Zhu, Jill A. Rosenfeld, Hoda Abdel-Hamid, Yulin Zhou, Zheng Jane Fan, Joyce E. Fox, Eugen Matthias Strehle, Linbo Yu, Deborah Barbouth, Sandra Donkervoort, Cathy A. Stevens, Alicia Vaglio, Roger L. Ladda
المصدر: American Journal of Medical Genetics Part A. :2139-2151
مصطلحات موضوعية: Genetics, Comparative Genomic Hybridization, Genotype, PITX2, Infant, Chromosome, Syndrome, Biology, Bioinformatics, Phenotype, DUX4, ANK2, Humans, Female, Deletion mapping, Chromosome Deletion, Chromosomes, Human, Pair 4, In Situ Hybridization, Fluorescence, Genetics (clinical), GRID2, Comparative genomic hybridization
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5
المؤلفون: Yiping Shen, Peining Li, Tian Jian Chen, Yueying Wang, David T. Miller, Bai-Lin Wu, Hongbo Zhu, Xiaofeng Hu, Hans C. Andersson, Jose E. Martinez, Tarachandra M. Narumanchi, Kangmo Lu, Bixia Xiang, Yao Shan Fan, Marilyn M. Li
المصدر: The Journal of Molecular Diagnostics. 12:204-212
مصطلحات موضوعية: Proband, Gene duplication, Etiology, Molecular Medicine, Clinical significance, Human genome, Computational biology, Microdeletion syndrome, Biology, Bioinformatics, Genome, Pathology and Forensic Medicine, Comparative genomic hybridization
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6
المصدر: Muscle & Nerve. 34:437-443
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Mitochondrial DNA, RNA, Mitochondrial, Physiology, Molecular Sequence Data, Exercise intolerance, Mitochondrion, Biology, medicine.disease_cause, DNA, Mitochondrial, Electron Transport, Cytosine, Cellular and Molecular Neuroscience, Muscular Diseases, Mitochondrial myopathy, Physiology (medical), Internal medicine, medicine, Respiratory muscle, Humans, Point Mutation, Gene, Genetics, Mutation, Exercise Tolerance, Base Sequence, Mitochondrial Myopathies, medicine.disease, Heteroplasmy, Pedigree, Endocrinology, RNA, RNA, Transfer, Lys, Female, Neurology (clinical), medicine.symptom, Thymine
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7
المؤلفون: Jose E. Martinez, Tian-Jian Chen, Paul Maertens, Wladimir Wertelecki, Yueying Wang, Glen L. Wilson, Xi-Yu He, Cathy M. Tuck-Muller
المصدر: American Journal of Medical Genetics Part A. :1274-1279
مصطلحات موضوعية: Male, Proband, Biology, Ribosomal Protein S6 Kinases, 90-kDa, Severity of Illness Index, Nuclear Family, Exon, Lateral ventricles, X Chromosome Inactivation, Intellectual Disability, Genotype, Coffin-Lowry Syndrome, Genetics, medicine, Humans, Allele, Alleles, Genetics (clinical), Sequence Deletion, Coffin–Lowry syndrome, Siblings, Brain, Exons, Syndrome, medicine.disease, Magnetic Resonance Imaging, Stop codon, Radiography, Mutagenesis, Insertional, Mutation, Mutation (genetic algorithm), Female
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8
المؤلفون: Duan-Jun Tan, Lee-Jun C. Wong, Tian-Jian Chen
المصدر: ELECTROPHORESIS. 25:2602-2610
مصطلحات موضوعية: Electrophoresis, Agar Gel, Genetics, Mitochondrial DNA, Homoplasmy, Polymorphism, Genetic, Mitochondrial disease, Point mutation, Clinical Biochemistry, Temperature, Biology, medicine.disease, DNA, Mitochondrial, Biochemistry, Molecular biology, Heteroplasmy, DNA sequencing, Analytical Chemistry, chemistry.chemical_compound, chemistry, Mutation, medicine, Humans, DNA, Temperature gradient gel electrophoresis, DNA Primers
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9
المؤلفون: Tian Jian Chen, Jeanne Meck, Lee-Jun C. Wong, Said Baidas, Valentin Kolev, Joel Imholte, Naigeng Qin
المصدر: American Journal of Medical Genetics. :383-387
مصطلحات موضوعية: Adult, Mosaicism, Meiosis II, Aneuploidy, Trisomy, Behcet's disease, Macrocytosis, Biology, Trisomy 8, medicine.disease, Miscarriage, Meiosis, Phenotype, Nondisjunction, Genetic, Immunology, medicine, Humans, Female, Stomatitis, Aphthous, Anemia, Macrocytic, Genetics (clinical), Chromosomes, Human, Pair 8
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec3c9dea2e3325746cd75d8c24696a53
https://doi.org/10.1002/ajmg.a.20390 -
10
المؤلفون: Cherng-Lih Perng, Cynthia J. Tifft, Tian-Jian Chen, Edith J. Chernoff, Lee-Jun C. Wong, Andrea L. Gropman, Donna M. Krasnewich
المصدر: American Journal of Medical Genetics. :377-382
مصطلحات موضوعية: Adult, Male, Proband, congenital, hereditary, and neonatal diseases and abnormalities, Mitochondrial DNA, Pathology, medicine.medical_specialty, Mitochondrial disease, Encephalopathy, Optic Atrophy, Hereditary, Leber, Biology, DNA, Mitochondrial, medicine, Humans, Point Mutation, Lactic Acid, Age of Onset, Child, Genetics (clinical), Dystonia, Genetics, Point mutation, medicine.disease, Pedigree, Muscle Spasticity, Child, Preschool, Lactic acidosis, Female, Age of onset
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3c32f0ece61de72466fbdbf9555876b
https://doi.org/10.1002/ajmg.a.20456