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Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.
Published in:
Clinical & Translational Medicine, 2016, v. 5, n. 1, p. 1, doi. 10.1186/s40169-016-0098-1
By:
- Siu, Wai‐Kwan;
- Lam, Ching‐Wan;
- Mak, Chloe Miu;
- Lau, Elizabeth Tak‐Kwong;
- Tang, Mary Hoi‐Yin;
- Tang, Wing‐Fai;
- Poon‐Mak, Rachel Sui‐Man;
- Lee, Chi‐Chiu;
- Hung, Se‐Fong;
- Leung, Patrick Wing‐Leung;
- Kwong, Karen Ling;
- Yau, Eric Kin‐Cheong;
- Ng, Grace Sui‐Fun;
- Fong, Nai‐Chung;
- Chan, Kwok‐Yin
Publication type:
Article
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.
Published in:
Clinical & Translational Medicine, 2016, v. 5, n. 1, p. 1, doi. 10.1186/s40169-016-0098-1
By:
- Siu, Wai-Kwan;
- Lam, Ching-Wan;
- Mak, Chloe;
- Lau, Elizabeth;
- Tang, Mary;
- Tang, Wing-Fai;
- Poon-Mak, Rachel;
- Lee, Chi-Chiu;
- Hung, Se-Fong;
- Leung, Patrick;
- Kwong, Karen;
- Yau, Eric;
- Ng, Grace;
- Fong, Nai-Chung;
- Chan, Kwok-Yin
Publication type:
Article
Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: Report and a review of literature Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature.
Published in:
American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1309, doi. 10.1002/ajmg.a.35909
By:
- Liu, Anthony P.Y.;
- Tang, Wing Fai;
- Lau, Elizabeth T.;
- Chan, Kelvin Y.K.;
- Kan, Anita S.Y.;
- Wong, Kar Yin;
- Tso, Winnie W.Y.;
- Jalal, Khair;
- Lee, So Lun;
- Chau, Christy S.K.;
- Chung, Brian H.Y.
Publication type:
Article
The Clinical Impact of Chromosomal Microarray on Paediatric Care in Hong Kong.
Published in:
PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109629
By:
- Tao, Victoria Q.;
- Chan, Kelvin Y. K.;
- Chu, Yoyo W. Y.;
- Mok, Gary T. K.;
- Tan, Tiong Y.;
- Yang, Wanling;
- Lee, So Lun;
- Tang, Wing Fai;
- Tso, Winnie W. Y.;
- Lau, Elizabeth T.;
- Kan, Anita S. Y.;
- Tang, Mary H.;
- Lau, Yu-lung;
- Chung, Brian H. Y.
Publication type:
Article
Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis.
Published in:
2019
By:
- Gill, Harinder;
- Ip, Ho-Wan;
- Yim, Rita;
- Tang, Wing-Fai;
- Pang, Herbert H.;
- Lee, Paul;
- Leung, Garret M. K.;
- Li, Jamilla;
- Tang, Karen;
- So, Jason C. C.;
- Leung, Rock Y. Y.;
- Li, Jun;
- Panagioutou, Gianni;
- Lam, Clarence C. K.;
- Kwong, Yok-Lam
Publication type:
journal article
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder--implications of a copy number variation involving DPP10.
Published in:
Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0136-x
By:
- Annisa Shui Lam Mak;
- Annie Ting Gee Chiu;
- Gordon Ka Chun Leung;
- Christopher Chun Yu Mak;
- Yoyo Wing Yiu Chu;
- Gary Tsz Kin Mok;
- Wing Fai Tang;
- Kelvin Yuen Kwong Chan;
- Mary Hoi Yin Tang;
- Elizabeth Tak-Kwong Lau Yim;
- Kin Wai So;
- Victoria Qinchen Tao;
- Cheuk Wing Fung;
- Virginia Chun Nei Wong;
- Uddin, Mohammed;
- So Lun Lee;
- Marshall, Christian R.;
- Scherer, Stephen W.;
- Anita Sik Yau Kan;
- Brian Hon Yin Chung
Publication type:
Article

Found: 6

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.

Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: Report and a review of literature Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature.

The Clinical Impact of Chromosomal Microarray on Paediatric Care in Hong Kong.

Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis.

Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder--implications of a copy number variation involving DPP10.