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1كتاب إلكتروني
المؤلفون: Perrot, AndreasAff10, Rickert-Sperling, SilkeAff11
المساهمون: Crusio, Wim E., Series EditorAff1, Dong, Haidong, Series EditorAff2, Radeke, Heinfried H., Series EditorAff3, Rezaei, Nima, Series EditorAff4, Steinlein, Ortrud, Series EditorAff5, Xiao, Junjie, Series EditorAff6, Rickert-Sperling, Silke, editorAff7, Kelly, Robert G., editorAff8, Haas, Nikolaus, editorAff9
المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:505-534
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2كتاب إلكتروني
المؤلفون: Aranega, Amelia E.Aff10, Franco, DiegoAff10
المساهمون: Crusio, Wim E., Series EditorAff1, Dong, Haidong, Series EditorAff2, Radeke, Heinfried H., Series EditorAff3, Rezaei, Nima, Series EditorAff4, Steinlein, Ortrud, Series EditorAff5, Xiao, Junjie, Series EditorAff6, Rickert-Sperling, Silke, editorAff7, Kelly, Robert G., editorAff8, Haas, Nikolaus, editorAff9
المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:313-339
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3كتاب إلكتروني
المؤلفون: Pfitzer, ConstanzeAff10, Schmitt, Katharina R. L.Aff10, Benson, Woodrow D.Aff11
المساهمون: Crusio, Wim E., Series EditorAff1, Dong, Haidong, Series EditorAff2, Radeke, Heinfried H., Series EditorAff3, Rezaei, Nima, Series EditorAff4, Steinlein, Ortrud, Series EditorAff5, Xiao, Junjie, Series EditorAff6, Rickert-Sperling, Silke, editorAff7, Kelly, Robert G., editorAff8, Haas, Nikolaus, editorAff9
المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:937-945
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4كتاب إلكتروني
المؤلفون: Perrot, AndreasAff10, Rickert-Sperling, SilkeAff11
المساهمون: Crusio, Wim E., Series EditorAff1, Dong, Haidong, Series EditorAff2, Radeke, Heinfried H., Series EditorAff3, Rezaei, Nima, Series EditorAff4, Steinlein, Ortrud, Series EditorAff5, Xiao, Junjie, Series EditorAff6, Rickert-Sperling, Silke, editorAff7, Kelly, Robert G., editorAff8, Haas, Nikolaus, editorAff9
المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:705-717
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5دورية أكاديمية
المصدر: Neuropsychiatric Disease and Treatment, Vol Volume 20, Pp 325-339 (2024)
مصطلحات موضوعية: autism, zic1, zic2, zic3, cerebellum, biomarkers., Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
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6دورية أكاديميةDetection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects
المصدر: Pharmacogenomics and Personalized Medicine, Vol Volume 16, Pp 173-181 (2023)
مصطلحات موضوعية: congenital heart disease, whole-exome sequencing, pld1, zic3, prenatal diagnosis, Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
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7كتاب إلكتروني
المؤلفون: Copp, Andrew J.Aff4, Aff5, Stanier, PhilipAff4, Greene, Nicholas D. E.Aff4, Pang, Dachling, Section editorAff6, Wang, Kyu-Chang, Section editorAff7, Thompson, Dominic, Section editorAff8
المساهمون: Di Rocco, Concezio, editorAff1, Pang, Dachling, editorAff2, Rutka, James T., editorAff3
المصدر: Textbook of Pediatric Neurosurgery. :2275-2294
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8دورية أكاديمية
المؤلفون: Deqin Chen, Yangfan Fan, Fang Wan
المصدر: Cancer Cell International, Vol 20, Iss 1, Pp 1-14 (2020)
مصطلحات موضوعية: Breast cancer, IGBP1-AS1, miR-24-1, ZIC3, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Cytology, QH573-671
وصف الملف: electronic resource
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9دورية أكاديمية
المؤلفون: Brianda A. Hernandez-Moran, Andrew S. Papanastasiou, David Parry, Alison Meynert, Philippe Gautier, Graeme Grimes, Ian R. Adams, Violeta Trejo-Reveles, Hemant Bengani, Margaret Keighren, Ian J. Jackson, David J. Adams, David R. FitzPatrick, Joe Rainger
المصدر: Genes, Vol 13, Iss 10, p 1797 (2022)
مصطلحات موضوعية: anophthalmia, X-chromosome, X-ray induced allele, linkage analysis, Zic3, genome wide analysis, Genetics, QH426-470
وصف الملف: electronic resource
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10دورية أكاديمية
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