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Expanded Newborn Screening for Inborn Errors of Metabolism in Hong Kong: Results and Outcome of a 7 Year Journey.
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.
Item in Clipboard
Clinical and molecular characterization study of Chinese Kabuki syndrome in Hong Kong.
So PL, Luk HM, Yu KPT, Cheng SSW, Hau EWL, Ho SKL, Lam STS, Lo IFM.
So PL, et al. Among authors: hau ewl.
Am J Med Genet A. 2021 Mar;185(3):675-686. doi: 10.1002/ajmg.a.62003. Epub 2020 Dec 13.
Am J Med Genet A. 2021.
PMID: 33314698
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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
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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.
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Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.
Tong TM, Hau EW, Lo IF, Chan DH, Lam ST.
Tong TM, et al.
Chin Med J (Engl). 2005 Sep 20;118(18):1499-506.
Chin Med J (Engl). 2005.
PMID: 16232326
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