نتائج البحث - Bai-Lin Wu
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Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis حسب Irene Mademont‐Soler, Carmen Morales, Anna Soler, J. M. Martínez‐Crespo, Yinchen Shen, Ester Margarit, Núria Clusellas, María Obón, Bai‐Lin Wu, Aurora Sánchez
منشور في 2012Artigo -
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Global DNA hypomethylation is associated with NTD‐affected pregnancy: A case‐control study حسب Xiaoli Chen, Jin Guo, Yunping Lei, Jizhen Zou, Xiaolin Lü, Yihua Bao, Lihua Wu, Jianxin Wu, Xiaoying Zheng, Yiping Shen, Bai‐Lin Wu, Ting Zhang
منشور في 2010Artigo -
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Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration حسب Florian Constanty, Bai‐Lin Wu, Ke-Hsuan Wei, I-Ting Lin, Julia Dallmann, Stefan Günther, Till Lautenschlaeger, Rashmi Priya, Shih-Lei Lai, Didier Y. R. Stainier, Arica Beisaw
منشور في 2025Artigo -
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Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development حسب Thị Kim Tuyền Đặng, Wenfeng Duan, Bin Yu, Dali Tong, Connie Cheng, Y F Zhang, Weiwei Wu, K Ye, W X Zhang, Meng Wu, Bai-Lin Wu, Yu An, Zilong Qiu, Bo Wu
منشور في 2017Artigo -
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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss حسب Pu Dai, Qi Li, Deliang Huang, Yongyi Yuan, Dongyang Kang, David T. Miller, Hong Shao, Qingwen Zhu, Jia He, Fei Yu, Xin Liu, Bing Han, Huijun Yuan, Orah S. Platt, Dongyi Han, Bai-Lin Wu
منشور في 2008Artigo -
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Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation حسب Bixia Xiang, Hongbo Zhu, Yiping Shen, David T. Miller, Kangmo Lu, Xiao Hu, Hans C. Andersson, Tarachandra M. Narumanchi, Yueying Wang, José E. Martínez, Bai-Lin Wu, Peining Li, Marilyn M. Li, Tian-Jian Chen, Yao‐Shan Fan
منشور في 2010Artigo -
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Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions حسب Andrew Dauber, Yongguo Yu, Michael C. Turchin, Charleston W. K. Chiang, Yan Meng, Ellen W. Demerath, Sanjay R. Patel, Stephen S. Rich, Jerome I. Rotter, Pamela J. Schreiner, James Wilson, Yiping Shen, Bai-Lin Wu, Joel N. Hirschhorn
منشور في 2011Artigo -
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Homozygous <i>PLCB1</i> deletion associated with malignant migrating partial seizures in infancy حسب Annapurna Poduri, Sameer S. Chopra, Edward Neilan, Princess C. Elhosary, Manju A. Kurian, Esther Meyer, Brenda J. Barry, Omar Khwaja, Mustafa A. Salih, Tommy Stödberg, Ingrid E. Scheffer, Eamonn R. Maher, Mustafa Şahin, Bai‐Lin Wu, Gerard T. Berry, Christopher A. Walsh, Jonathan Picker, Sanjeev V. Kothare
منشور في 2012Artigo -
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Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies حسب Shuhua Xu, Xianyong Yin, Shilin Li, Wenfei Jin, Haiyi Lou, Ling Yang, Xiaohong Gong, Hongyan Wang, Yiping Shen, Xuedong Pan, Yungang He, Yajun Yang, Yi Wang, Wenqing Fu, Yu An, Jiucun Wang, Jingze Tan, Ji Qian, Xiaoli Chen, Xin Zhang, Yangfei Sun, Xuejun Zhang, Bai-Lin Wu, Jin Li
منشور في 2009Artigo -
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Association between Microdeletion and Microduplication at 16p11.2 and Autism حسب Lauren A. Weiss, Yiping Shen, Joshua M. Korn, Dan E. Arking, David T. Miller, Ragnheiður Fossdal, Evald Sæmundsen, Hreinn Stefánsson, Todd Green, Orah S. Platt, Douglas M. Ruderfer, Christopher A. Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E. Tanzi, Hreinn Stefánsson, Susan L. Santangelo, James F. Gusella, Pamela Sklar, Bai-Lin Wu, Mark J. Daly
منشور في 2008Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Medicine
Internal medicine
Psychiatry
Genome
Mutation
Phenotype
Psychology
Autism
Copy-number variation
Genotype
Neuroscience
Allele
Autism spectrum disorder
Population
Single-nucleotide polymorphism
Cell biology
Endocrinology
Evolutionary biology
Gene expression
Pregnancy
Allele frequency
Audiology
Chemistry
Chromosome
Cohort
Embryo
Environmental health