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X
Tsang, Mandy Ho-Yin
62  Ergebnisse:
Personensuche X
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1

Successful transition from insulin to sulphonylurea in a ch..:

Poon, Sarah Wing-yiu ; Chung, Brian Hon-yin ; Tsang, Mandy Ho-yin.
Clinical Pediatric Endocrinology.  31 (2022)  3 - p. 168-171 , 2022
Link: https://doi.org/10.1297/..
 
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2

Exome sequencing in paediatric patients with movement disor..:

Kwong, Anna Ka-Yee ; Tsang, Mandy Ho-Yin ; Fung, Jasmine Lee-Fong...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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3

Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neuro..:

Chai, Guoliang ; Webb, Alice ; Li, Chen...
Neuron.  109 (2021)  2 - p. 241-256.e9 , 2021
Link: https://doi.org/10.1016/..
 
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4

Primary coenzyme Q10 deficiency-7: expanded phenotypic spec..:

Yu, Mullin Ho-Chung ; Tsang, Mandy Ho-Yin ; Lai, Sophie...
npj Genomic Medicine.  4 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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5

Comprehensive analysis of recessive carrier status using ex..:

Chau, Jeffrey Fong Ting ; Yu, Mullin Ho Chung ; Chui, Martin Man Chun...
npj Genomic Medicine.  7 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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6

Actionable pharmacogenetic variants in Hong Kong Chinese ex..:

Yu, Mullin Ho Chung ; Chan, Marcus Chun Yin ; Chung, Claudia Ching Yan...
PLOS Genetics.  17 (2021)  2 - p. e1009323 , 2021
Link: https://doi.org/10.1371/..
 
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7

Actionable secondary findings in 1116 Hong Kong Chinese bas..:

Yu, Mullin Ho Chung ; Mak, Christopher Chun Yu ; Fung, Jasmine Lee Fong...
Journal of Human Genetics.  66 (2020)  6 - p. 637-641 , 2020
Link: https://doi.org/10.1038/..
 
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8

Identification of mutations in the PI3K-AKT-mTOR signalling..:

Yeung, Kit San ; Tso, Winnie Wan Yee ; Ip, Janice Jing Kun...
Molecular Autism.  8 (2017)  1 - p. , 2017
Link: https://doi.org/10.1186/..
 
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9

Successful transition from insulin to sulphonylurea in a ch..:

Poon, Sarah Wing-yiu ; Chung, Brian Hon-yin ; Tsang, Mandy Ho-yin.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297163/.  , 2022
Link: http://www.ncbi.nlm.nih...
 
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10

Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neuro..:

Chai, Guoliang ; Webb, Alice ; Li, Chen...
qt6w53352f.  , 2021
Link: https://escholarship.org..
 
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11

Primary coenzyme Q10 deficiency-7: expanded phenotypic spec..:

Yu, Mullin Ho-Chung ; Tsang, Mandy Ho-Yin ; Lai, Sophie...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683205/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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12

Exome sequencing in paediatric patients with movement disor..:

Anna Ka-Yee Kwong ; Mandy Ho-Yin Tsang ; Jasmine Lee-Fong Fung...
https://doi.org/10.1186/s13023-021-01688-6.  , 2021
Link: https://doi.org/10.1186/..
 
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13

Additional file 1 of Exome sequencing in paediatric patient..:

Anna Ka-Yee Kwong (9989370) ; Mandy Ho-Yin Tsang (9989373) ; Jasmine Lee-Fong Fung (9989376)...
https://figshare.com/articles/journal_contribution/Additional_file_1_of_Exome_sequencing_in_paediatric_patients_with_movement_disorders/13578936.  , 2021
Link: https://doi.org/10.6084/..
 
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14

Comprehensive analysis of recessive carrier status using ex..:

Jeffrey Fong Ting Chau ; Mullin Ho Chung Yu ; Martin Man Chun Chui...
https://doi.org/10.1038/s41525-022-00287-z.  , 2022
Link: https://doi.org/10.1038/..
 
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15

Actionable pharmacogenetic variants in Hong Kong Chinese ex..:

Mullin Ho Chung Yu ; Marcus Chun Yin Chan ; Claudia Ching Yan Chung...
https://doi.org/10.1371/journal.pgen.1009323.  , 2021
Link: https://doi.org/10.1371/..
 
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