Chung BHY - Search Results

1

Importance of cascade family screening and precision medicine for patients with familial hyperkalaemia: a case report.

Lam HY, Chan EYH, Tung JYL, Lee SLK, Fung JLF, Lee M, Chung BHY, Ma ALT. Lam HY, et al. Among authors: chung bhy. Hong Kong Med J. 2022 Oct;28(5):406-408. doi: 10.12809/hkmj219513. Hong Kong Med J. 2022. PMID: 38232967 Free article. No abstract available.

2

Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children.

Yu TC, Liu AP, Lun KS, Chung BH, Yung TC. Yu TC, et al. Hong Kong Med J. 2016 Aug;22(4):314-9. doi: 10.12809/hkmj154653. Epub 2016 Jun 3. Hong Kong Med J. 2016. PMID: 27256466 Free article.

3

Molecular diagnosis of severe combined immunodeficiency using whole-exome sequencing.

Yang WL, Lau YL, Lee PP, Chung BH, Yang J. Yang WL, et al. Hong Kong Med J. 2018 Jun;24 Suppl 3(3):15-17. Hong Kong Med J. 2018. PMID: 29937439 Free article. No abstract available.

4

Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey.

Mak CC, Leung GK, Mok GT, Yeung KS, Yang W, Fung CW, Chan SH, Lee SL, Lee NC, Pfundt R, Lau YL, Chung BH. Mak CC, et al. NPJ Genom Med. 2018 Aug 6;3:19. doi: 10.1038/s41525-018-0056-5. eCollection 2018. NPJ Genom Med. 2018. PMID: 30109123 Free PMC article.

5

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).

Leung GKC, Mak CCY, Fung JLF, Wong WHS, Tsang MHY, Yu MHC, Pei SLC, Yeung KS, Mok GTK, Lee CP, Hui APW, Tang MHY, Chan KYK, Liu APY, Yang W, Sham PC, Kan ASY, Chung BHY. Leung GKC, et al. Among authors: chung bhy. BMC Med Genomics. 2018 Oct 25;11(1):93. doi: 10.1186/s12920-018-0409-z. BMC Med Genomics. 2018. PMID: 30359267 Free PMC article.

6

Clinical and genetic profile of congenital long QT syndrome in Hong Kong: a 20-year experience in paediatrics.

Kwok SY, Liu AP, Chan CY, Lun KS, Fung JL, Mak CC, Chung BH, Yung TC. Kwok SY, et al. Hong Kong Med J. 2018 Dec;24(6):561-570. doi: 10.12809/hkmj187487. Epub 2018 Dec 3. Hong Kong Med J. 2018. PMID: 30530868 Free article.

7

A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35.

Fung JLF, Tsang MHY, Leung GKC, Yeung KS, Mak CCY, Fung CW, Chan SHS, Yu MHC, Chung BHY. Fung JLF, et al. Among authors: chung bhy. Parkinsonism Relat Disord. 2019 Jun;63:42-45. doi: 10.1016/j.parkreldis.2019.01.013. Epub 2019 Jan 17. Parkinsonism Relat Disord. 2019. PMID: 30670339

8

The different facets of "culture" in genetic counseling: A situated analysis of genetic counseling in Hong Kong.

Zayts O, Shipman H, Fung JL, Liu AP, Kwok SY, Tsai AC, Yung TC, Chung BH. Zayts O, et al. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):187-195. doi: 10.1002/ajmg.c.31699. Epub 2019 May 2. Am J Med Genet C Semin Med Genet. 2019. PMID: 31046193 Review.

9

Coffin-Lowry syndrome in Chinese.

Fung JLF, Rethanavelu K, Luk HM, Ho MSP, Lo IFM, Chung BHY. Fung JLF, et al. Among authors: chung bhy. Am J Med Genet A. 2019 Oct;179(10):2043-2048. doi: 10.1002/ajmg.a.61323. Epub 2019 Aug 9. Am J Med Genet A. 2019. PMID: 31400053

10

Phenotypic and mutational spectrum of 21 Chinese patients with Alström syndrome.

Rethanavelu K, Fung JLF, Chau JFT, Pei SLC, Chung CCY, Mak CCY, Luk HM, Chung BHY. Rethanavelu K, et al. Among authors: chung bhy, chung ccy. Am J Med Genet A. 2020 Feb;182(2):279-288. doi: 10.1002/ajmg.a.61412. Epub 2019 Nov 22. Am J Med Genet A. 2020. PMID: 31755649

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