Resultados de procura - Garcia-Barcelo, Maria-Mercè
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Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population por Miao, Xiaoping, Garcia‐Barceló, Maria‐Mercè, So, Man‐ting, Yuk‐yu Leon, Thomas, Ko‐chun Lau, Danny, Liu, Ting‐Ting, Kin‐Wai Chan, Edwin, Chuen‐Leung Lan, Lawrence, Kak‐yuen Wong, Kenneth, Chi‐hang Lui, Vincent, Kwong‐hang Tam, Paul, Garcia‐Barceló, Maria‐Mercè, Kwong‐hang Tam, Paul
Publicado 2007Text -
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AB113. The first genetic study on congenital choledochal dilatation (CCD) implicates extracellular matrix proteins por Garcia-Barceló, Maria-Mercè, Wong, John Kwong Leong, Ngo, Ngoc Diem, Tran, Ngoc Son, Nguyen, Thanh Liem, Nguyen, Liem, Sham, Pak, Cherny, Stacey, Tam, Paul
Publicado 2015Text -
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Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype por Cheng, William Wai-Chun, Tang, Clara Sze-Man, Gui, Hong-Sheng, So, Man-Ting, Lui, Vincent Chi-Hang, Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè
Publicado 2015Text -
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Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis por Cheng, Guo, Chung, Patrick Ho-Yu, Chan, Edwin Kin-Wai, So, Man-Ting, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado 2017Text -
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Gene Network Analysis of Candidate Loci for Human Anorectal Malformations por Wong, Emily H. M., Ng, Chun-Laam, Lui, Vincent Chi-Hang, So, Man-ting, Cherny, Stacey S., Sham, Pak-Chung, Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado 2013Text -
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Conditional deletion of platelet derived growth factor receptor alpha (Pdgfra) in urorectal mesenchyme causes mesenchyme apoptosis and urorectal developmental anomalies in mice por Qian, Chen, Wu, Zhongluan, Ng, Roy Chun-Laam, Garcia-Barceló, Maria-Mercè, Yuan, Zheng-Wei, Wong, Kenneth Kak Yuen, Tam, Paul Kwong Hang, Lui, Vincent Chi Hang
Publicado 2018Text -
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Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia por Cui, Long, Wong, Emily Hoi-Man, Cheng, Guo, Firmato de Almeida, Manoel, So, Man-Ting, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado 2013Text -
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Haplotype Analysis Reveals a Possible Founder Effect of RET Mutation R114H for Hirschsprung's Disease in the Chinese Population por Cornes, Belinda K., Tang, Clara S., Leon, Thomas Y. Y., Hui, Kenneth J. W. S., So, Man-Ting, Miao, Xiaoping, Cherny, Stacey S., Sham, Pak C., Tam, Paul K. H., Garcia-Barcelo, Maria-Merce
Publicado 2010Text -
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Sacral agenesis: a pilot whole exome sequencing and copy number study por Porsch, Robert M., Merello, Elisa, De Marco, Patrizia, Cheng, Guo, Rodriguez, Laura, So, Manting, Sham, Pak C., Tam, Paul K., Capra, Valeria, Cherny, Stacey S., Garcia-Barcelo, Maria-Mercè, Campbell, Desmond D.
Publicado 2016Text -
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A random forest-based framework for genotyping and accuracy assessment of copy number variations por Zhuang, Xuehan, Ye, Rui, So, Man-Ting, Lam, Wai-Yee, Karim, Anwarul, Yu, Michelle, Ngo, Ngoc Diem, Cherny, Stacey S, Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè, Tang, Clara Sze-man, Sham, Pak Chung
Publicado 2020Text -
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Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing por Tang, Clara SM, Zhuang, Xuehan, Lam, Wai-Yee, Ngan, Elly Sau-Wai, Hsu, Jacob Shujui, Michelle, YU, Man-Ting, SO, Cherny, Stacey S, Ngo, Ngoc Diem, Sham, Pak C, Tam, Paul KH, Garcia-Barcelo, Maria-Mercè
Publicado 2018Text -
13
Cancer gene mutations in congenital pulmonary airway malformation patients por Hsu, Jacob Shujui, Zhang, Ruizhong, Yeung, Fanny, Tang, Clara S.M., Wong, John K.L., So, Man-Ting, Xia, Huimin, Sham, Pak, Tam, Paul K., Li, Miaoxin, Wong, Kenneth K.Y., Garcia-Barcelo, Maria-Mercè
Publicado 2019Text -
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Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism por Liu, Wei, Wong, John KL, He, Qiuming, Wong, Emily HM, Tang, Clara SM, Zhang, Ruizhong, So, Man-ting, Wong, Kenneth KY, Nicholls, John, Cherny, Stacey S, Sham, Pak C, Tam, Paul K, Garcia-Barcelo, Maria-Mercè, Xia, Huimin
Publicado 2015Text -
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Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes por Wong, John K. L., Campbell, Desmond, Ngo, Ngoc Diem, Yeung, Fanny, Cheng, Guo, Tang, Clara S. M., Chung, Patrick H. Y., Tran, Ngoc Son, So, Man-ting, Cherny, Stacey S., Sham, Pak C., Tam, Paul K., Garcia-Barcelo, Maria-Mercè
Publicado 2016Text -
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Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors por Tang, Clara Sze Man, Mononen, Mimmi, Lam, Wai-Yee, Jin, Sheng Chih, Zhuang, Xuehan, Garcia-Barcelo, Maria-Mercè, Lin, Qiongfen, Yang, Yujia, Sahara, Makoto, Eroglu, Elif, Chien, Kenneth R., Hong, Haifa, Tam, Paul Kwong Hang, Gruber, Peter J.
Publicado 2022Text -
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Whole-genome analysis of noncoding genetic variations identifies multiscale regulatory element perturbations associated with Hirschsprung disease por Fu, Alexander Xi, Lui, Kathy Nga-Chu, Tang, Clara Sze-Man, Ng, Ray Kit, Lai, Frank Pui-Ling, Lau, Sin-Ting, Li, Zhixin, Garcia-Barcelo, Maria-Mercè, Sham, Pak-Chung, Tam, Paul Kwong-Hang, Ngan, Elly Sau-Wai, Yip, Kevin Y.
Publicado 2020Text -
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AB080. Genetic findings provide insight of biliary atresia patient complexity por Cheng, Guo, Garcia-Barceló, Maria-Mercè, Chung, Patrick Ho-Yu, Tang, Wai-Kiu, Man Wong, Emily Hoi, Chan, Edwin Kin-Wai, So, Man-Ting, Ngo, Diem Ngoc, Tran, Ngoc Son, Nguyen, Pham Anh Hoa, Sham, Pak-Chung, Cherny, Stacey S., Nicholls, John M., Tam, Paul Kwong-Hang
Publicado 2015Text -
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Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans por Ngan, Elly Sau-Wai, Garcia-Barceló, Maria-Mercè, Yip, Benjamin Hon-Kei, Poon, Hiu-Ching, Lau, Sin-Ting, Kwok, Carmen Ka-Man, Sat, Eric, Sham, Mai-Har, Wong, Kenneth Kak-Yuen, Wainwright, Brandon J., Cherny, Stacey S., Hui, Chi-Chung, Sham, Pak Chung, Lui, Vincent Chi-Hang, Tam, Paul Kwong-Hang
Publicado 2011Text -
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Functional polymorphisms in the promoter of BRCA1 influences transcription and are associated with decreased risk for breast cancer in Chinese women por Chan, Kelvin Yuen-Kwong, Liu, Wei, Long, Ji-Rong, Yip, Shea-Ping, Chan, Sum-Yin, Shu, Xiao-Ou, Chua, Daniel Tsin-Tien, Cheung, Annie Nga-Yin, Ching, Johannes Chi-Yun, Cai, Hui, Au, Gordon Kwok-Hung, Chan, Miranda, Foo, William, Ngan, Hextan Yuen-Sheung, Gao, Yu-Tang, Ngan, Elly Sau-Wai, Garcia-Barceló, Maria-Mercè, Zheng, Wei, Khoo, Ui-Soon
Publicado 2008Text