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1دورية أكاديمية
المؤلفون: Liang-Liang Fan, Zhuang-Zhuang Yuan, Zi-Jun Jiao, Hui Zeng, Yi-Feng Yang, Zhi-Ping Tan
المصدر: Genes and Diseases, Vol 9, Iss 6, Pp 1412-1414 (2022)
مصطلحات موضوعية: Medicine (General), R5-920, Genetics, QH426-470
وصف الملف: electronic resource
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2
المؤلفون: Zi-Jun Jiao, Jie-Yuan Jin, Liang-Liang Fan, Zhuang-Zhuang Yuan, Yi Dong, Rong Xiang, Dan-Dong Bi
المصدر: All Life. 14:874-880
مصطلحات موضوعية: General Neuroscience, General Agricultural and Biological Sciences, General Biochemistry, Genetics and Molecular Biology
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3
المؤلفون: Liang-Liang Fan, Zhuang-Zhuang Yuan, Zi-Jun Jiao, Hui Zeng, Yi-Feng Yang, Zhi-Ping Tan
المصدر: Genesdiseases. 9(6)
مصطلحات موضوعية: Cell Biology, Molecular Biology, Biochemistry, Genetics (clinical)
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4
المؤلفون: Rong Xiang, Fang Yu, Jie-Yuan Jin, Juyu Tang, Zhuang-Zhuang Yuan, Zi-Jun Jiao
المصدر: Bioscience Reports
مصطلحات موضوعية: Male, 0301 basic medicine, Heterozygote, Candidate gene, Heredity, prolonged protein, DNA Mutational Analysis, Biophysics, Biochemistry, Proximal symphalangism, Frameshift mutation, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Asian People, Finger Joint, Ankylosis, medicine, Humans, Genetic Predisposition to Disease, NOG, Family history, Child, Frameshift Mutation, Molecular Biology, Research Articles, Exome sequencing, Sanger sequencing, Genetics, Whole Genome Sequencing, Gene Expression & Regulation, business.industry, Genomics, Cell Biology, medicine.disease, frameshift variant, Pedigree, Conductive hearing loss, Phenotype, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation, symbols, Female, Joint Diseases, Carrier Proteins, business, Interphalangeal Joint
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc799506cda982d5c2410e141f138bb0
https://doi.org/10.1042/bsr20200509 -
5
المؤلفون: Yi Dong, Zi-Jun Jiao, Jie Li, Jie-Yuan Jin, Rong Xiang, Dan-Yu Liu
المصدر: BioMed Research International
BioMed Research International, Vol 2020 (2020)مصطلحات موضوعية: 0301 basic medicine, Proband, Male, Pathology, medicine.medical_specialty, Article Subject, Cosegregation, DNA Mutational Analysis, 030105 genetics & heredity, Compound heterozygosity, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Neuromuscular junction, 03 medical and health sciences, Camptodactyly, Retinal Diseases, medicine, Humans, Child, Unilateral ptosis, Muscle contracture, Arthrogryposis, Arthrogryposis multiplex congenita, Ophthalmoplegia, General Immunology and Microbiology, business.industry, Metalloendopeptidases, General Medicine, Pedigree, 030104 developmental biology, medicine.anatomical_structure, Mutation, Medicine, medicine.symptom, business, Research Article
وصف الملف: text/xhtml
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6
المؤلفون: Fang, Yu, Jie-Yuan, Jin, Ji-Qiang, He, Liang-Liang, Fan, Zi-Jun, Jiao, Pan-Feng, Wu, Ju-Yu, Tang, Rong, Xiang
المصدر: International journal of clinical and experimental pathology. 12(8)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::6986b90444c7a3621153a7377d8dc336
https://pubmed.ncbi.nlm.nih.gov/31934135 -
7دورية أكاديمية
المؤلفون: Zhuang-Zhuang Yuan, Fang Yu, Jie-Yuan Jin, Zi-Jun Jiao, Ju-Yu Tang, Rong Xiang
المصدر: Bioscience Reports; Jun2020, Vol. 40 Issue 6, p1-8, 8p
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8دورية أكاديمية
المؤلفون: Jie-Yuan Jin, Dan-Yu Liu, Zi-Jun Jiao, Yi Dong, Jie Li, Rong Xiang
المصدر: BioMed Research International; 5/23/2020, p1-6, 6p
مصطلحات موضوعية: FINGER abnormalities, ELBOW abnormalities, ARTHROGRYPOSIS, GENETIC mutation, PROTEOLYTIC enzymes, SEQUENCE analysis