E-LIB Suche - Ergebnisse für: Leung, Gordon K. C.

1

Rapid whole-exome sequencing facilitates precision medicine..:

Chung, Claudia C.Y. ; Leung, Gordon K.C. ; Mak, Christopher C.Y....
The Lancet Regional Health - Western Pacific. 1 (2020) - p. 100001 , 2020

Link: https://doi.org/10.1016/..

2

Diagnostic value of whole‐exome sequencing in Chinese pedia..:

Tsang, Mandy H. Y. ; Chiu, Annie T. G. ; Kwong, Bernard M. H....
Molecular Genetics & Genomic Medicine. 8 (2020) 5 - p. , 2020

Link: https://doi.org/10.1002/..

3

A significant inflation in TGM6 genetic risk casts doubt in..:

Fung, Jasmine L.F. ; Tsang, Mandy H.Y. ; Leung, Gordon K.C....
Parkinsonism & Related Disorders. 63 (2019) - p. 42-45 , 2019

Link: https://doi.org/10.1016/..

4

Genetic landscape of RASopathies in Chinese: Three decades'..:

Yu, Kris P. T. ; Luk, Ho‐Ming ; Leung, Gordon K. C....
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 181 (2019) 2 - p. 208-217 , 2019

Link: https://doi.org/10.1002/..

5

Identifying the genetic causes for prenatally diagnosed str..:

Leung, Gordon K C ; Mak, Christopher C Y ; Fung, Jasmine L F...
BMC Medical Genomics. 11 (2018) 1 - p. , 2018

Link: https://doi.org/10.1186/..

6

Integrating Functional Analysis in the Next-Generation Sequ..:

Leung, Gordon K. C. ; Luk, H. M. ; Tang, Vincent H. M....
Scientific Reports. 8 (2018) 1 - p. , 2018

Link: https://doi.org/10.1038/..

7

Cover Image, Volume 173A, Number 9, September 2017:

Kruszka, Paul ; Porras, Antonio R. ; Addissie, Yonit A....
American Journal of Medical Genetics Part A. 173 (2017) 9 - p. , 2017

Link: https://doi.org/10.1002/..

8

Noonan syndrome in diverse populations:

Kruszka, Paul ; Porras, Antonio R. ; Addissie, Yonit A....
American Journal of Medical Genetics Part A. 173 (2017) 9 - p. 2323-2334 , 2017

Link: https://doi.org/10.1002/..

9

De novo large rare copy-number variations contribute to con..:

Mak, Christopher C Y ; Chow, Pak Cheong ; Liu, Anthony P Y...
npj Genomic Medicine. 1 (2016) 1 - p. , 2016

Link: https://doi.org/10.1038/..

10

CFTRfounder mutation causes protein trafficking defects in ..:

Leung, Gordon K. C. ; Ying, Dingge ; Mak, Christopher C. Y....
Molecular Genetics & Genomic Medicine. 5 (2016) 1 - p. 40-49 , 2016

Link: https://doi.org/10.1002/..

11

Before and after – Nutritional transformation of dysmorphis..:

Chiu, Annie T.G. ; Zhu, Lixing ; Mok, Gary T.K....
European Journal of Medical Genetics. 59 (2016) 11 - p. 573-576 , 2016

Link: https://doi.org/10.1016/..

12

Cellular Dielectric Spectroscopy: A Powerful New Approach t..:

Ciambrone, Gary J. ; Liu, Vivian F. ; Lin, Deborah C....
SLAS Discovery. 9 (2004) 6 - p. 467-480 , 2004

Link: https://doi.org/10.1177/..

13

Isoprenylcysteine Carboxyl Methyltransferase Deficiency in ..:

Bergo, Martin O. ; Leung, Gordon K. ; Ambroziak, Patricia...
Journal of Biological Chemistry. 276 (2001) 8 - p. 5841-5845 , 2001

Link: https://doi.org/10.1074/..

14

Targeted Inactivation of the Isoprenylcysteine Carboxyl Met..:

Bergo, Martin O. ; Leung, Gordon K. ; Ambroziak, Patricia...
Journal of Biological Chemistry. 275 (2000) 23 - p. 17605-17610 , 2000

Link: https://doi.org/10.1074/..

15

Rapid whole-exome sequencing facilitates precision medicine..:

Chung, Claudia C.Y ; Leung, Gordon K.C ; Mak, Christopher C.Y...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8315561/. , 2020

Link: http://www.ncbi.nlm.nih...