Showing 1 - 7 results of 7 for search 'Anita S Y Kan', query time: 0.03s
Refine Results
-
1
Revealing parental mosaicism: the hidden answer to the recurrence of apparent de novo variants by Mianne Lee, Adrian C. Y. Lui, Joshua C. K. Chan, Phoenix H. L. Doong, Anna K. Y. Kwong, Christopher C. Y. Mak, Raymond H. W. Li, Anita S. Y. Kan, Brian H. Y. Chung
Published 2023-10-01
Article -
2
Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes by Kunfeng Bai, Cheuk-Lun Lee, Xiaofeng Liu, Jianlin Li, Dandan Cao, Li Zhang, Duanlin Hu, Hong Li, Yanqing Hou, Yue Xu, Anita S. Y. Kan, Ka-Wang Cheung, Ernest H. Y. Ng, William S. B. Yeung, Philip C. N. Chiu
Published 2022-02-01
Article -
3
Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept by Mianne Lee, Anna K. Y. Kwong, Martin M. C. Chui, Jeffrey F. T. Chau, Christopher C. Y. Mak, Sandy L. K. Au, Hei Man Lo, Kelvin Y. K. Chan, Vicente A. Yépez, Julien Gagneur, Anita S. Y. Kan, Brian H. Y. Chung
Published 2022-12-01
Article -
4
Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong. by Anita S Y Kan, Elizabeth T Lau, W F Tang, Sario S Y Chan, Simon C K Ding, Kelvin Y K Chan, C P Lee, Pui Wah Hui, Brian H Y Chung, K Y Leung, Teresa Ma, Wing C Leung, Mary H Y Tang
Published 2014-01-01
Article -
5
Dysregulation of the CD147 complex confers defective placental development: A pathogenesis of early‐onset preeclampsia by Cheuk‐Lun Lee, Zhilong Chen, Qingqing Zhang, Yue Guo, Vivian W.Y. Ng, Baozhen Zhang, Kunfeng Bai, Degong Ruan, Anita S.Y. Kan, Ka‐Wang Cheung, Annisa S.L. Mak, William S.B. Yeung, Rui Su, Qing Yang, Min Chen, Mei‐Rong Du, Zhang Jian, Xiujun Fan, Philip C.N. Chiu
Published 2022-06-01
Article -
6
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) by 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
Published 2018-10-01
Article -
7
The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes by 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
Published 2020-07-01
Article