Cheng SSW - Search Results

1

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: cheng ssw. Prenat Diagn. 2021 Aug;41(9):1089-1100. doi: 10.1002/pd.5998. Epub 2021 Jul 3. Prenat Diagn. 2021. PMID: 34185329 Review.

2

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: cheng ssw. 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

3

Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.

Cheng SSW, Chan KYK, Leung KKP, Au PKC, Tam WK, Li SKM, Luk HM, Kan ASY, Chung BHY, Lo IFM, Tang MHY. Cheng SSW, et al. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):196-207. doi: 10.1002/ajmg.c.31697. Epub 2019 Mar 23. Am J Med Genet C Semin Med Genet. 2019. PMID: 30903683 Review.

4

CHARGE syndrome in nine patients from China.

Cheng SSW, Luk HM, Chan DKH, Lo IFM. Cheng SSW, et al. Am J Med Genet A. 2020 Jan;182(1):15-19. doi: 10.1002/ajmg.a.61398. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729160

5

Adult Chinese twins with Kenny-Caffey syndrome type 2: A potential age-dependent phenotype and review of literature.

Cheng SSW, Chan PKJ, Luk HM, Mok MT, Lo IFM. Cheng SSW, et al. Am J Med Genet A. 2021 Feb;185(2):636-646. doi: 10.1002/ajmg.a.61991. Epub 2020 Dec 1. Am J Med Genet A. 2021. PMID: 33263187 Review.

6

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: cheng ssw. 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

7

An adult Chinese patient with developmental delay with short stature, dysmorphic features, and sparse hair (Loucks-Innes syndrome).

Cheng SSW, Luk HM, Lo IFM. Cheng SSW, et al. Am J Med Genet A. 2021 Jun;185(6):1925-1931. doi: 10.1002/ajmg.a.62164. Epub 2021 Mar 11. Am J Med Genet A. 2021. PMID: 33704902

8

Genotype and phenotype in 18 Chinese patients with Coffin-Siris syndrome.

Cheng SSW, Luk HM, Mok MT, Leung SS, Lo IFM. Cheng SSW, et al. Am J Med Genet A. 2021 Jul;185(7):2250-2261. doi: 10.1002/ajmg.a.62187. Epub 2021 Mar 26. Am J Med Genet A. 2021. PMID: 33768696

9

Old and new perspectives on Neurofibromatosis type 1: Clinical and molecular characterization of 832 patients from a single centre over 16 years.

Ho SK, Luk HM, Ng SY, Yu KP, Cheng SS, Ng PP, Mok MT, Hau EW, Lo IF. Ho SK, et al. Eur J Med Genet. 2022 Apr;65(4):104474. doi: 10.1016/j.ejmg.2022.104474. Epub 2022 Feb 28. Eur J Med Genet. 2022. PMID: 35240321

10

Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders.

Cao Y, Luk HM, Zhang Y, Chau MHK, Xue S, Cheng SSW, Li AM, Chong JSC, Leung TY, Dong Z, Choy KW, Lo IFM. Cao Y, et al. Among authors: cheng ssw. Front Genet. 2022 Apr 14;13:803088. doi: 10.3389/fgene.2022.803088. eCollection 2022. Front Genet. 2022. PMID: 35495136 Free PMC article.

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