E-LIB Suche - Ergebnisse für: Fung, Jasmine L.F.

1

Socio-economic costs of rare diseases and the risk of finan..:

Chung, Claudia C.Y. ; Ng, Nicole Y.T. ; Ng, Yvette N.C....
The Lancet Regional Health - Western Pacific. 34 (2023) - p. 100711 , 2023

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

2

Evaluating the Health-Related Quality of Life of the Rare D..:

Ng, Yvette N.C. ; Ng, Nicole Y.T. ; Fung, Jasmine L.F....
Value in Health. 25 (2022) 9 - p. 1624-1633 , 2022

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

3

Refractory thrombocytopenia and myelofibrosis in a novel KD..:

Wong, G. Y. ; Hung, Zita G. K. ; Ho, Karin K. H....
Pediatric Blood & Cancer. 70 (2022) 4 - p. , 2022

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

4

'Do language and culturereallymatter?': A trans‐disciplinar..:

Zayts‐Spence, Olga ; Fung, Jasmine L. F. ; Chung, Brian H. Y.
Journal of Genetic Counseling. 30 (2021) 1 - p. 75-84 , 2021

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

5

Understanding and perception of direct‐to‐consumer genetic ..:

Hui, Vivian C. C. ; Li, H. C. ; Chow, Josh H. K....
Journal of Genetic Counseling. 30 (2021) 6 - p. 1640-1648 , 2021

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

6

Further expanding the clinical phenotype in Bainbridge-Rope..:

Yu, Kris Pui-Tak ; Luk, Ho-Ming ; Fung, Jasmine L.F...
European Journal of Medical Genetics. 64 (2021) 1 - p. 104107 , 2021

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

7

Client Service Receipt Inventory as a standardised tool for..:

Chung, Claudia C. Y. ; Fung, Jasmine L. F. ; Lui, Adrian C. Y....
Scientific Reports. 11 (2021) 1 - p. , 2021

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

8

A three-year follow-up study evaluating clinical utility of..:

Fung, Jasmine L. F. ; Yu, Mullin H. C. ; Huang, Shushu...
npj Genomic Medicine. 5 (2020) 1 - p. , 2020

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

9

Reply: MN1 gene loss-of-function mutation causes cleft pala..:

Vegas, Nancy ; Low, Karen ; Mak, Christopher C Y...
Brain. 144 (2020) 2 - p. e19-e19 , 2020

Link: https://doi.org/10.1093/..

10

A case of G1013R FBN1 mutation: A potential genotype–phenot..:

Willis, Brooke R. ; Lee, Mianne ; Rethanavelu, Kavitha...
American Journal of Medical Genetics Part A. 182 (2020) 6 - p. 1329-1335 , 2020

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

11

The KLHL40 c.1516A>C is a Chinese‐specific founder mutation..:

Yeung, Kit San ; Yu, Florrie N. Y. ; Fung, Cheuk Wing...
Molecular Genetics & Genomic Medicine. 8 (2020) 7 - p. , 2020

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

12

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/..

13

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/..

14

Delineation of molecular findings by whole-exome sequencing..:

Tsang, Mandy H.Y. ; Kwong, Anna K.Y. ; Chan, Kate L.S....
Human Genomics. 14 (2020) 1 - p. , 2020

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

15

Rubinstein–Taybi syndrome in diverse populations:

Tekendo‐Ngongang, Cedrik ; Owosela, Babajide ; Fleischer, Nicole...
American Journal of Medical Genetics Part A. 182 (2020) 12 - p. 2939-2950 , 2020

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