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1دورية أكاديمية
المؤلفون: Yanping Ruan, Yaqi Wang, Jianhui Guo, Tingting Man, Xiaoyan Hao, Xiaoxue Zhou, Chenyu Wang, Hanyu Deng, Jing Li, Zhiyong Zou, Yihua He
المصدر: Ecotoxicology and Environmental Safety, Vol 276, Iss , Pp 116328- (2024)
مصطلحات موضوعية: Cohort study, Conotruncal heart defects, Air pollution, O3, Environmental pollution, TD172-193.5, Environmental sciences, GE1-350
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S0147651324004044Test; https://doaj.org/toc/0147-6513Test
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2دورية أكاديمية
المصدر: Cam & Sakura Medical Journal, Vol 3, Iss 3, Pp 107-112 (2023)
مصطلحات موضوعية: child, conotruncal heart diseases, extracardiac manifestations, Medicine
وصف الملف: electronic resource
العلاقة: https://jag.journalagent.com/z4/download_fulltext.asp?pdir=csmedj&un=CSM-36844Test; https://doaj.org/toc/2791-8823Test
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3دورية أكاديمية
المؤلفون: Alaaeldin G. Fayez, PhD, Nora N. Esmaiel, PhD, Engy A. Ashaat, MD, Miral M. Refeat, PhD, Randa S. Lotfy, PhD, Haiam Abdel Raouf, PhD, Mona O. El Ruby, MD
المصدر: Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp 1244-1253 (2023)
مصطلحات موضوعية: Akt, Conotruncal heart defects, Drug design, PIP3 antagonist, Pleckstrin homology domain, Signal transduction pathway, Medicine (General), R5-920
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S1658361223000653Test; https://doaj.org/toc/1658-3612Test
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4دورية أكاديمية
المؤلفون: Harvey, Drayton C, Baer, Rebecca J, Bandoli, Gretchen, Chambers, Christina D, Jelliffe‐Pawlowski, Laura L, Kumar, S Ram
المصدر: Journal of the American Heart Association. 11(2)
مصطلحات موضوعية: Perinatal Period - Conditions Originating in Perinatal Period, Substance Misuse, Cardiovascular, Heart Disease, Brain Disorders, Congenital Structural Anomalies, Alcoholism, Alcohol Use and Health, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Good Health and Well Being, Endocardial Cushions, Female, Heart Defects, Congenital, Humans, Infant, Live Birth, Pregnancy, Prenatal Exposure Delayed Effects, Retrospective Studies, Risk Factors, alcohol, cardiac development, cardiac outflow tract, cardiovascular disease risk factors, congenital cardiac defect, conotruncal defect, endocardial cushion defect, pregnancy, Cardiorespiratory Medicine and Haematology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/07f9t3mkTest
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5دورية أكاديمية
المؤلفون: Marta Camprubí-Camprubí, Joan Sanchez-de-Toledo
المصدر: Frontiers in Pediatrics, Vol 11 (2023)
مصطلحات موضوعية: conotruncal abnormalities, fallot tetralogy, DORV, transposition of great arteries, sub aortic stenosis, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2023.1323167/fullTest; https://doaj.org/toc/2296-2360Test
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6دورية أكاديمية
المؤلفون: Edwards, Jonathan J, Rouillard, Andrew D, Fernandez, Nicolas F, Wang, Zichen, Lachmann, Alexander, Shankaran, Sunita S, Bisgrove, Brent W, Demarest, Bradley, Turan, Nahid, Srivastava, Deepak, Bernstein, Daniel, Deanfield, John, Giardini, Alessandro, Porter, George, Kim, Richard, Roberts, Amy E, Newburger, Jane W, Goldmuntz, Elizabeth, Brueckner, Martina, Lifton, Richard P, Seidman, Christine E, Chung, Wendy K, Tristani-Firouzi, Martin, Yost, H Joseph, Ma'ayan, Avi, Gelb, Bruce D
المصدر: JACC. Basic to translational science. 5(4)
مصطلحات موضوعية: CHD, congenital heart disease, CORUM, Comprehensive Resource of Mammalian Protein Complexes, CRISPR, clustered regularly interspaced short palindromic repeats, CTD, conotruncal defect, GOBP, Gene Ontology biological processes, HHE, high heart expression, HLHS, hypoplastic left heart syndrome, HTX, heterotaxy, LVOTO, left ventricular outflow tract obstruction, MGI, Mouse Genome Informatics, PCGC, Pediatric Cardiac Genomics Consortium, PPI, protein-protein interaction, congenital heart disease, systems biology, translational genomics, CHD, CORUM, Comprehensive Resource of Mammalian Protein Complexes, CRISPR, clustered regularly interspaced short palindromic repeats, CTD, conotruncal defect, GOBP, Gene Ontology biological processes, HHE, high heart expression, HLHS, hypoplastic left heart syndrome, HTX, heterotaxy, LVOTO, left ventricular outflow tract obstruction, MGI, Mouse Genome Informatics, PCGC, Pediatric Cardiac Genomics Consortium, PPI, protein-protein interaction, Cardiorespiratory Medicine and Haematology, Clinical Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/25s8k1msTest
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7دورية أكاديمية
المؤلفون: Drayton C. Harvey, Riya Verma, Brandon Sedaghat, Brooke E. Hjelm, Sarah U. Morton, Jon G. Seidman, S. Ram Kumar
المصدر: Frontiers in Cardiovascular Medicine, Vol 10 (2023)
مصطلحات موضوعية: tetralogy of fallot, exome sequencing, congenital heart defect, de novo variants, conotruncal defects, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fcvm.2023.1249605/fullTest; https://doaj.org/toc/2297-055XTest
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8دورية أكاديمية
المؤلفون: Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware
المصدر: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 18 (2023)
مصطلحات موضوعية: chromosomal microarray, congenital heart disease, conotruncal defects, genomics, neurodevelopment, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2047-9980Test
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9دورية أكاديمية
المؤلفون: Zhao, Yingjie, Diacou, Alexander, Johnston, H Richard, Musfee, Fadi I, McDonald-McGinn, Donna M, McGinn, Daniel, Crowley, T Blaine, Repetto, Gabriela M, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R, Kates, Wendy R, Digilio, M Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J, Murphy, Kieran C, Murphy, Clodagh M, Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J, Shprintzen, Robert J, Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Consortium, International 22q11 2 Brain and Behavior, Antonarakis, Stylianos E, Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P, Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S, Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther DA, Vergaelen, Elfi, Warren, Steve T, Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E, Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob AS, Gothelf, Doron, Zackai, Elaine, Agopian, AJ, Gur, Raquel E, Bassett, Anne S, Emanuel, Beverly S, Goldmuntz, Elizabeth, Mitchell, Laura E, Wang, Tao, Morrow, Bernice E
المصدر: American Journal of Human Genetics. 106(1)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Epidemiology, Health Sciences, Clinical Research, Human Genome, Heart Disease, Cardiovascular, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Case-Control Studies, Chromosome Deletion, Chromosomes, Human, Pair 22, Cohort Studies, Female, Genome-Wide Association Study, Heart Defects, Congenital, Humans, Linkage Disequilibrium, Male, Phenotype, Polymorphism, Single Nucleotide, Proto-Oncogene Mas, Segmental Duplications, Genomic, International 22q11.2 Brain and Behavior Consortium, CRKL, DiGeorge syndrome, TBX1, chromosome 22q11.2 deletion syndrome, complex trait, congenital heart disease, conotruncal heart defects, copy number variation, genetic association, genetic modifier, haploinsufficiency, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/38b9f8cxTest
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10دورية أكاديمية
المؤلفون: Ayşe Keleş, Osman Yılmaz, Özge Yücel Çelik, Gülşah Dağdeviren, Gülşah Aynaoğlu Yıldız, Aykan Yücel, Dilek Şahin
المصدر: Gülhane Tıp Dergisi, Vol 64, Iss 3, Pp 222-228 (2022)
مصطلحات موضوعية: conotruncal heart anomalies, fetal echocardiography, prenatal diagnosis, ultrasonography, Medicine
وصف الملف: electronic resource
العلاقة: http://gulhanemedj.org/archives/archive-detail/article-preview/characteristics-of-fetalTest-conotruncal-heart-anomali/52868; https://doaj.org/toc/2146-8052Test