Canlyniadau Chwilio - Bai‐Lin Wu
- Dangos 1 - 20 canlyniadau o 32
- Ewch i'r Dudalen Nesaf
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<i>VANGL2</i>Mutations in Human Cranial Neural-Tube Defects gan Yunping Lei, Ting Zhang, Hong Li, Bai Lin Wu, Jin Li, Hong Yan Wang
Cyhoeddwyd 2010Carta -
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Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray‐based analysis gan Irene Mademont‐Soler, Carmen Morales, Anna Soler, J. M. Martínez‐Crespo, Yinchen Shen, Ester Margarit, Núria Clusellas, María Obón, Bai‐Lin Wu, Aurora Sánchez
Cyhoeddwyd 2012Artigo -
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Global DNA hypomethylation is associated with NTD‐affected pregnancy: A case‐control study gan 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
Cyhoeddwyd 2010Artigo -
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Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration gan 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
Cyhoeddwyd 2025Artigo -
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Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development gan 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
Cyhoeddwyd 2017Artigo -
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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss gan 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
Cyhoeddwyd 2008Artigo -
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Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation gan 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
Cyhoeddwyd 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 gan 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
Cyhoeddwyd 2011Artigo -
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Homozygous <i>PLCB1</i> deletion associated with malignant migrating partial seizures in infancy gan 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
Cyhoeddwyd 2012Artigo -
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Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies gan 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
Cyhoeddwyd 2009Artigo -
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Association between Microdeletion and Microduplication at 16p11.2 and Autism gan 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
Cyhoeddwyd 2008Artigo
Offerynnau Chwilio:
Pynciau Perthynol
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