Hasil Pencarian - H.C. Yu

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  1. 1
    Global seamless tidal simulation using a 3D unstructured-grid model (SCHISM v5.10.0)

    Global seamless tidal simulation using a 3D unstructured-grid model (SCHISM v5.10.0) oleh Y. J. Zhang, T. Fernandez-Montblanc, W. Pringle, H.-C. Yu, L. Cui, S. Moghimi

    Diterbitkan 2023-05-01
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  2. 2
    A cross-scale study for compound flooding processes during Hurricane Florence

    A cross-scale study for compound flooding processes during Hurricane Florence oleh F. Ye, W. Huang, Y. J. Zhang, S. Moghimi, E. Myers, S. Pe'eri, H.-C. Yu

    Diterbitkan 2021-06-01
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  3. 3
    Record of the Late Paleozoic Ice Age From Tarim, China

    Record of the Late Paleozoic Ice Age From Tarim, China oleh H. C. Yu, K. F. Qiu, M. Li, M. Santosh, Z. G. Zhao, Y. Q. Huang

    Diterbitkan 2020-11-01
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  4. 4
    Early intervention with faecal microbiota transplantation: an effective means to improve growth performance and the intestinal development of suckling piglets

    Early intervention with faecal microbiota transplantation: an effective means to improve growth performance and the intestinal development of suckling piglets oleh C.S. Cheng, H.K. Wei, P. Wang, H.C. Yu, X.M. Zhang, S.W. Jiang, J. Peng

    Diterbitkan 2019-01-01
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  5. 5
    Cardiology Training in Brazil and Developed Countries: Some Ideas for Improvement

    Cardiology Training in Brazil and Developed Countries: Some Ideas for Improvement oleh Lucas Colombo Godoy, Michael E. Farkouh, Isabela C. K. Abud Manta, Talia F. Dalçóquio, Remo Holanda de Mendonça Furtado, Eric H. C. Yu, Carlos Gun, José Carlos Nicolau

    Diterbitkan 2019-11-01
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  6. 6
    Evaluating High‐Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses

    Evaluating High‐Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses oleh Martin M. C. Chui, Christopher C. Y. Mak, Mullin H. C. Yu, Sandra Y. Y. Wong, Kin‐Shing Lun, Tak‐Cheung Yung, Anna K. Y. Kwong, Pak‐Cheong Chow, Brian H. Y. Chung

    Diterbitkan 2023-02-01
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  7. 7
    Diagnostic value of whole‐exome sequencing in Chinese pediatric‐onset neuromuscular patients

    Diagnostic value of whole‐exome sequencing in Chinese pediatric‐onset neuromuscular patients oleh Mandy H. Y. Tsang, Annie T. G. Chiu, Bernard M. H. Kwong, Rui Liang, Mullin H. C. Yu, Kit‐San Yeung, Wetor H. L. Ho, Christopher C. Y. Mak, Gordon K. C. Leung, Steven L. C. Pei, Jasmine L. F. Fung, Virginia C. N. Wong, Francesco Muntoni, Brian H. Y. Chung, Sophelia H. S. Chan

    Diterbitkan 2020-05-01
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  8. 8
    Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

    Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) oleh Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Wilfred H S Wong, Mandy H Y Tsang, Mullin H C Yu, Steven L C Pei, K S Yeung, Gary T K Mok, C P Lee, Amelia P W Hui, Mary H Y Tang, Kelvin Y K Chan, Anthony P Y Liu, Wanling Yang, P C Sham, Anita S Y Kan, Brian H Y Chung

    Diterbitkan 2018-10-01
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  9. 9
    The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes

    The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes oleh Kit San Yeung, Florrie N. Y. Yu, Cheuk Wing Fung, Sheila Wong, Hencher H. C. Lee, Sharon T. H. Fung, Genevieve P. G. Fung, Kwok Yin Leung, Wai Hang Chung, Yun Ting Lee, Vivian K. S. Ng, Mullin H. C. Yu, Jasmine L. F. Fung, Mandy H. Y. Tsang, Kelvin Y. K. Chan, Sophelia H. S. Chan, Anita S. Y. Kan, Brian H. Y. Chung

    Diterbitkan 2020-07-01
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  10. 10
    Integrating Functional Analysis in the Next-Generation Sequencing Diagnostic Pipeline of RASopathies

    Integrating Functional Analysis in the Next-Generation Sequencing Diagnostic Pipeline of RASopathies oleh Gordon K. C. Leung, H. M. Luk, Vincent H. M. Tang, W. W. Gao, Christopher C. Y. Mak, Mullin H. C. Yu, W. L. Wong, Yoyo W. Y. Chu, W. L. Yang, Wilfred H. S. Wong, Alvin C. H. Ma, Anskar Y. H. Leung, D. Y. Jin, Kelvin Y. K. Chan, Judith Allanson, Ivan F. M. Lo, Brian H. Y. Chung

    Diterbitkan 2018-02-01
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  11. 11
    Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population

    Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population oleh Mandy H.Y. Tsang, Anna K.Y. Kwong, Kate L.S. Chan, Jasmine L.F. Fung, Mullin H.C. Yu, Christopher C.Y. Mak, Kit-San Yeung, Richard J.T. Rodenburg, Jan A.M. Smeitink, Rachel Chan, Thomas Tsoi, Joannie Hui, Shelia S.N Wong, Shuk-Mui Tai, Victor C.M. Chan, Che-Kwan Ma, Sharon T.H. Fung, Shun-Ping Wu, W.K. Chak, Brian H.Y. Chung, Cheuk-Wing Fung

    Diterbitkan 2020-09-01
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  12. 12
    Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs

    Rapid whole-exome sequencing facilitates precision medicine in paediatric rare disease patients and reduces healthcare costs oleh Claudia C.Y. Chung, Gordon K.C. Leung, Christopher C.Y. Mak, Jasmine L.F. Fung, Mianne Lee, Steven L.C. Pei, Mullin H.C. Yu, Vivian C.C. Hui, Joshua C.K. Chan, Jeffrey F.T. Chau, Marcus C.Y. Chan, Mandy H.Y. Tsang, Wilfred H.S. Wong, Joanna Y.L. Tung, Kin Shing Lun, Yiu Ki Ng, Cheuk Wing Fung, Mabel S.C. Wong, Rosanna M.S. Wong, Yu Lung Lau, Godfrey C.F. Chan, So Lun Lee, Kit San Yeung, Brian H.Y. Chung

    Diterbitkan 2020-08-01
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