Lo IF - Search Results

1

A prenatal case of split-hand malformation associated with 17p13.3 triplication - a dilemma in genetic counseling.

Luk HM, Wong VC, Lo IF, Chan KY, Lau ET, Kan AS, Tang MH, Tang WF, She WM, Chu YW, Sin WK, Chung BH. Luk HM, et al. Among authors: lo if. Eur J Med Genet. 2014 Feb;57(2-3):81-4. doi: 10.1016/j.ejmg.2013.12.005. Epub 2013 Dec 28. Eur J Med Genet. 2014. PMID: 24380768

2

Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation.

Yeung KS, Chee YY, Luk HM, Kan AS, Tang MH, Lau ET, Shuen AY, Lo IF, Chan KY, Chung BH. Yeung KS, et al. Among authors: lo if. Am J Med Genet A. 2014 Oct;164A(10):2521-8. doi: 10.1002/ajmg.a.36670. Epub 2014 Jul 16. Am J Med Genet A. 2014. PMID: 25044945

3

Mechanisms for the Generation of Two Quadruplications Associated with Split-Hand Malformation.

Gu S, Posey JE, Yuan B, Carvalho CM, Luk HM, Erikson K, Lo IF, Leung GK, Pickering CR, Chung BH, Lupski JR. Gu S, et al. Among authors: lo if. Hum Mutat. 2016 Feb;37(2):160-4. doi: 10.1002/humu.22929. Epub 2015 Dec 2. Hum Mutat. 2016. PMID: 26549411 Free PMC article.

4

Angelman syndrome in Hong Kong Chinese: A 20 years' experience.

Luk HM, Lo IF. Luk HM, et al. Among authors: lo if. Eur J Med Genet. 2016 Jun;59(6-7):315-9. doi: 10.1016/j.ejmg.2016.05.003. Epub 2016 May 9. Eur J Med Genet. 2016. PMID: 27174604

5

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.

6

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. 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

7

Coffin-Lowry syndrome in Chinese.

Fung JLF, Rethanavelu K, Luk HM, Ho MSP, Lo IFM, Chung BHY. Fung JLF, et al. 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

8

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

9

Rubinstein-Taybi syndrome in Chinese population with four novel mutations.

Yu PT, Luk HM, Lo IFM. Yu PT, et al. Am J Med Genet A. 2021 Jan;185(1):267-273. doi: 10.1002/ajmg.a.61922. Epub 2020 Oct 16. Am J Med Genet A. 2021. PMID: 33063428

10

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

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