المؤلفون: Perrot, Andreas^Aff10, Rickert-Sperling, Silke^Aff11

المساهمون: Crusio, Wim E., Series Editor^Aff1, Dong, Haidong, Series Editor^Aff2, Radeke, Heinfried H., Series Editor^Aff3, Rezaei, Nima, Series Editor^Aff4, Steinlein, Ortrud, Series Editor^Aff5, Xiao, Junjie, Series Editor^Aff6, Rickert-Sperling, Silke, editor^Aff7, Kelly, Robert G., editor^Aff8, Haas, Nikolaus, editor^Aff9

المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:505-534

المؤلفون: Aranega, Amelia E.^Aff10, Franco, Diego^Aff10

المساهمون: Crusio, Wim E., Series Editor^Aff1, Dong, Haidong, Series Editor^Aff2, Radeke, Heinfried H., Series Editor^Aff3, Rezaei, Nima, Series Editor^Aff4, Steinlein, Ortrud, Series Editor^Aff5, Xiao, Junjie, Series Editor^Aff6, Rickert-Sperling, Silke, editor^Aff7, Kelly, Robert G., editor^Aff8, Haas, Nikolaus, editor^Aff9

المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:313-339

المؤلفون: Pfitzer, Constanze^Aff10, Schmitt, Katharina R. L.^Aff10, Benson, Woodrow D.^Aff11

المساهمون: Crusio, Wim E., Series Editor^Aff1, Dong, Haidong, Series Editor^Aff2, Radeke, Heinfried H., Series Editor^Aff3, Rezaei, Nima, Series Editor^Aff4, Steinlein, Ortrud, Series Editor^Aff5, Xiao, Junjie, Series Editor^Aff6, Rickert-Sperling, Silke, editor^Aff7, Kelly, Robert G., editor^Aff8, Haas, Nikolaus, editor^Aff9

المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:937-945

المؤلفون: Perrot, Andreas^Aff10, Rickert-Sperling, Silke^Aff11

المساهمون: Crusio, Wim E., Series Editor^Aff1, Dong, Haidong, Series Editor^Aff2, Radeke, Heinfried H., Series Editor^Aff3, Rezaei, Nima, Series Editor^Aff4, Steinlein, Ortrud, Series Editor^Aff5, Xiao, Junjie, Series Editor^Aff6, Rickert-Sperling, Silke, editor^Aff7, Kelly, Robert G., editor^Aff8, Haas, Nikolaus, editor^Aff9

المصدر: Congenital Heart Diseases: The Broken Heart : Clinical Features, Human Genetics and Molecular Pathways. 1441:705-717

المؤلفون: Li H, Cui J, Hu C, Luo X, Hao Y

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

Relation: https://www.dovepress.com/identification-and-analysis-of-zic-related-genes-in-cerebellum-of-auti-peer-reviewed-fulltext-article-NDT; https://doaj.org/toc/1178-2021

URL الوصول: https://doaj.org/article/b9c6bbb3d26642f09e1c0c63275dfe6f

المؤلفون: Cai R, Tan Y, Wang M, Yu H, Wang J, Ren Z, Dong Z, He Y, Li Z, Lin L, Gu Y

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

Relation: https://www.dovepress.com/detection-of-novel-pathogenic-variants-in-two-families-with-recurrent--peer-reviewed-fulltext-article-PGPM; https://doaj.org/toc/1178-7066

URL الوصول: https://doaj.org/article/32689a044672474d85c89cfb0eafa003

المؤلفون: Copp, Andrew J.^{Aff4, Aff5}, Stanier, Philip^Aff4, Greene, Nicholas D. E.^Aff4, Pang, Dachling, Section editor^Aff6, Wang, Kyu-Chang, Section editor^Aff7, Thompson, Dominic, Section editor^Aff8

المساهمون: Di Rocco, Concezio, editor^Aff1, Pang, Dachling, editor^Aff2, Rutka, James T., editor^Aff3

المصدر: Textbook of Pediatric Neurosurgery. :2275-2294

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

Relation: http://link.springer.com/article/10.1186/s12935-020-01214-x; https://doaj.org/toc/1475-2867

URL الوصول: https://doaj.org/article/79d5f9447e9048ecba4a8709d7cbab5e

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

Relation: https://www.mdpi.com/2073-4425/13/10/1797; https://doaj.org/toc/2073-4425

URL الوصول: https://doaj.org/article/24813787dfdf4334be55a7a9617139c1

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