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1Academic Journal
المؤلفون: Ting Zhang, Xiaoling Duan, Ying Feng, Wei Jiang, Xueqin Hou, Ling Liu, Qinrong Huang, Xiang Tang, Li Lin, Mingqiang Zhang, Liang Tao, Guoqing Liu, Yuxia Chen, Nong Xiao
المصدر: Frontiers in Pediatrics, Vol 10 (2022)
مصطلحات موضوعية: early rehabilitation, critical illness, child, tertiary care centers, survey, Pediatrics, RJ1-570
وصف الملف: electronic resource
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2Academic Journal
المؤلفون: Qinrong, Huang, Yuxia, Chen, Ling, Liu, Huayu, Luo, Lei, Xu, Xiaoli, Li, Nong, Xiao
المساهمون: Chongqing Medical University
المصدر: Developmental Medicine & Child Neurology ; volume 65, issue 4, page 563-570 ; ISSN 0012-1622 1469-8749
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3Academic Journal
المؤلفون: Qinrong, Huang, Yuxia, Chen, Ling, Liu, Huayu, Luo, Lei, Xu, Xiaoli, Li, Nong, Xiao
المصدر: Developmental Medicine & Child Neurology; Apr2023, Vol. 65 Issue 4, p563-570, 8p
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4
المؤلفون: Ting Zhang, Xiaoling Duan, Ying Feng, Wei Jiang, Xueqin Hou, Ling Liu, Qinrong Huang, Xiang Tang, Li Lin, Mingqiang Zhang, Liang Tao, Guoqing Liu, Yuxia Chen, Nong Xiao
مصطلحات موضوعية: Foetal Development and Medicine, Obstetrics and Gynaecology, Paediatrics, Paediatrics and Reproductive Medicine not elsewhere classified, early rehabilitation, critical illness, child, tertiary care centers, survey
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5
المؤلفون: Yuxia Chen, Xiang Tang, Ling Liu, Qinrong Huang, Li Lin, Guoqing Liu, Nong Xiao
المصدر: Genesdiseases. 9(5)
مصطلحات موضوعية: Cell Biology, Molecular Biology, Biochemistry, Genetics (clinical)
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6
المؤلفون: Hui Xiong, Zhe Tao, FeiFei Yue, Qinrong Huang, Nong Xiao
المصدر: European Journal of Medical Genetics. 64:104289
مصطلحات موضوعية: Heart Defects, Congenital, Male, Heterozygote, Nonsense mutation, medicine.disease_cause, Craniofacial Abnormalities, EHMT1, Neurodevelopmental disorder, Protein Domains, Intellectual Disability, Genetics, medicine, Humans, Missense mutation, Global developmental delay, Genetics (clinical), Kleefstra Syndrome, Mutation, business.industry, Infant, Histone-Lysine N-Methyltransferase, General Medicine, medicine.disease, Hypotonia, Phenotype, Child, Preschool, Female, Chromosome Deletion, medicine.symptom, Chromosomes, Human, Pair 9, business
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7
المؤلفون: Luying Cao, Ziyu Hua, Min Zhu, Qinrong Huang, Yu Zhang, Weixia Du, Yi He, Pinglan Deng, Hong Wei
المصدر: Endocrine. 69(1)
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, China, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Gene mutation, DEND syndrome, ABCC8, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Neonatal diabetes mellitus, Diabetes mellitus, Diabetes Mellitus, Medicine, Humans, Potassium Channels, Inwardly Rectifying, Molecular Biology, Retrospective Studies, biology, business.industry, Infant, Newborn, Infant, Permanent neonatal diabetes mellitus, IPEX syndrome, medicine.disease, Transient neonatal diabetes mellitus, 030220 oncology & carcinogenesis, Mutation, biology.protein, business