المؤلفون: Peng-Fei Zheng, Rui-Xing Yin, Guo-Xiong Deng, Yao-Zong Guan, Bi-Liu Wei, Chun-Xiao Liu

المصدر: BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-8 (2019)

مصطلحات موضوعية: Coronary artery disease, Ischemic stroke, XKR6, Single nucleotide polymorphism, rs7819412, Lipids, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12872-019-1179-z; https://doaj.org/toc/1471-2261

URL الوصول: https://doaj.org/article/e89307e98d564d78b75590f94c9c2a10

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المؤلفون: Zheng, Peng-Fei^Aff1, Yin, Rui-Xing^{Aff1, Aff2, Aff3}, Deng, Guo-Xiong^Aff1, Guan, Yao-Zong^Aff1, Wei, Bi-Liu^Aff1, Liu, Chun-Xiao^Aff1

المصدر: BMC Cardiovascular Disorders. 19(1)

المؤلفون: Herbert Schulz, Zuhal Yapici, Nihan Hande Akçakaya, Server Hande Çağlayan, Thomas Sander, Özlem Yalçın Çapan

المصدر: Epileptic Disorders. 19:217-221

مصطلحات موضوعية: Heart Defects, Congenital, Male, MIR597, Heart disease, Developmental Disabilities, Genetic counseling, 030204 cardiovascular system & hematology, Biology, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Intellectual disability, medicine, Humans, Abnormalities, Multiple, 030212 general & internal medicine, Copy-number variation, XKR6, Child, Genomic Copy Number Variation, Genetics, Absence Seizure, General Medicine, medicine.disease, Phenotype, Absence seizure, Epilepsy, Absence, Neurology, Epilepsy syndromes, Microcephaly, 8p23.1 Deletion Syndrome, Neurology (clinical), Chromosome Deletion, Chromosomes, Human, Pair 8

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b1e8a8c523fd8b7afa41c45d634a00
https://doi.org/10.1684/epd.2017.0906

المؤلفون: Guo-Xiong Deng, Peng-Fei Zheng, Yao-Zong Guan, Bi-Liu Wei, Chun-Xiao Liu, Rui-Xing Yin

المصدر: BMC Cardiovascular Disorders
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-8 (2019)

مصطلحات موضوعية: Male, lcsh:Diseases of the circulatory (Cardiovascular) system, rs7819412, Coronary Artery Disease, 030204 cardiovascular system & hematology, Gastroenterology, Brain Ischemia, Coronary artery disease, chemistry.chemical_compound, 0302 clinical medicine, Gene Frequency, Risk Factors, 030212 general & internal medicine, Ischemic stroke, Middle Aged, Lipids, 3. Good health, Cardiac surgery, Stroke, Cholesterol, Phenotype, Female, Cardiology and Cardiovascular Medicine, Research Article, medicine.medical_specialty, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Risk Assessment, 03 medical and health sciences, Internal medicine, medicine, Humans, SNP, Genetic Predisposition to Disease, cardiovascular diseases, XKR6, Allele, Allele frequency, Genetic Association Studies, Triglycerides, Aged, Angiology, Triglyceride, business.industry, Membrane Proteins, medicine.disease, Single nucleotide polymorphism, chemistry, lcsh:RC666-701, Case-Control Studies, business, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818e07edcc5be841a60c0edacff92af1
https://doi.org/10.1186/s12872-019-1179-z

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