Luk HM - Search Results

1

Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.

So PL, Hui ASY, Ma TWL, Shu W, Hui APW, Kong CW, Lo TK, Kan ANC, Kan EYL, Chong SC, Chung BHY, Luk HM, Choy KW, Kan ASY, Leung WC. So PL, et al. Among authors: luk hm. Genes (Basel). 2022 Nov 10;13(11):2088. doi: 10.3390/genes13112088. Genes (Basel). 2022. PMID: 36360323 Free PMC article.

2

Prenatal diagnosis of familial atretic encephalocele.

Lau WL, Yung WY, Leung WC, Kan A, Chan K, Luk HM, Kan E, Lam YY. Lau WL, et al. Among authors: luk hm. Ultrasound Obstet Gynecol. 2019 Aug;54(2):277-279. doi: 10.1002/uog.20109. Ultrasound Obstet Gynecol. 2019. PMID: 30151917 Free article. No abstract available.

3

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: luk hm. 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

4

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

5

Fibrodysplasia ossificans progressiva in Hong Kong-A case report series.

Chan JCK, Kuong EE, Chan JPK, Luk HM, Fung JLF, Tung JY, Chung BHY. Chan JCK, et al. Among authors: luk hm. Front Pediatr. 2023 Apr 25;11:1152731. doi: 10.3389/fped.2023.1152731. eCollection 2023. Front Pediatr. 2023. PMID: 37181433 Free PMC article.

6

Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities.

Hui PW, Mok YK, Luk HM, Au SLK, Lau EYT, Chung B, Kan ASY. Hui PW, et al. Among authors: luk hm. Prenat Diagn. 2023 Sep;43(10):1366-1369. doi: 10.1002/pd.6414. Epub 2023 Aug 2. Prenat Diagn. 2023. PMID: 37529930

7

Genetic association of retroesophageal left brachiocephalic vein.

Chan YM, Law KM, Poon LCY, Luk HM, Cheng YKY, Leung TY. Chan YM, et al. Among authors: luk hm. Ultrasound Obstet Gynecol. 2019 Dec;54(6):836-837. doi: 10.1002/uog.20275. Ultrasound Obstet Gynecol. 2019. PMID: 30937965 Free article. No abstract available.

8

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. 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

9

Integrating Functional Analysis in the Next-Generation Sequencing Diagnostic Pipeline of RASopathies.

Leung GKC, Luk HM, Tang VHM, Gao WW, Mak CCY, Yu MHC, Wong WL, Chu YWY, Yang WL, Wong WHS, Ma ACH, Leung AYH, Jin DY, Chan KYK, Allanson J, Lo IFM, Chung BHY. Leung GKC, et al. Among authors: luk hm. Sci Rep. 2018 Feb 5;8(1):2421. doi: 10.1038/s41598-018-20894-0. Sci Rep. 2018. PMID: 29402968 Free PMC article.

10

Genetic profile and clinical application of chromosomal microarray in children with intellectual disability in Hong Kong.

Chan PY, Luk HM, Lee FM, Lo IF. Chan PY, et al. Among authors: luk hm. Hong Kong Med J. 2018 Oct;24(5):451-459. doi: 10.12809/hkmj187260. Hong Kong Med J. 2018. PMID: 30262673 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

94 results

Search Page