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Expanded Newborn Screening for Inborn Errors of Metabolism in Hong Kong: Results and Outcome of a 7 Year Journey.
Belaramani KM, Chan TCH, Hau EWL, Yeung MCW, Kwok AMK, Lo IFM, Law THF, Wu H, Wong SSN, Lam SW, Ha GHY, Lau TPY, Wong TK, Or VWC, Wong RMS, Ming WL, Chow JCK, Yau EKC, Fu A, Chong JSC, Yau HC, Poon GWK, Ng KL, Chan KT, Lam YY, Hui J, Mak CM, Fung CW. Belaramani KM, et al. Among authors: hau ewl. Int J Neonatal Screen. 2024 Mar 11;10(1):23. doi: 10.3390/ijns10010023. Int J Neonatal Screen. 2024. PMID: 38535127 Free PMC article.
Prenatal phenotype of Kabuki syndrome: A case series and literature review.
So PL, Luk HM, Cheung KW, Hui W, Chung MY, Mak ASL, Lok WY, Yu KPT, Cheng SSW, Hau EWL, Ho S, Lam STS, Lo IFM. So PL, et al. Among authors: hau ewl. Prenat Diagn. 2021 Aug;41(9):1089-1100. doi: 10.1002/pd.5998. Epub 2021 Jul 3. Prenat Diagn. 2021. PMID: 34185329 Review.
Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong.
Yu KPT, Luk HM, Leung GKC, Mak CCY, Cheng SSW, Hau EWL, Chan DKH, Lam STS, Tong TMF, Chung BHY, Lo IFM. Yu KPT, et al. Among authors: hau ewl. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):208-217. doi: 10.1002/ajmg.c.31692. Epub 2019 Mar 21. Am J Med Genet C Semin Med Genet. 2019. PMID: 30896080
Prader--Willi syndrome: 16-year experience in Hong Kong.
Lo IF, Luk HM, Tong TM, Lai KK, Chan DH, Lam AC, Chan DK, Hau EW, Fung CO, Lam ST. Lo IF, et al. J Genet Genomics. 2012 Apr 20;39(4):191-4. doi: 10.1016/j.jgg.2012.02.005. J Genet Genomics. 2012. PMID: 22685788 No abstract available.