Lam ST - Search Results

1

Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.

Liu AP, Chow PC, Lee PP, Mok GT, Tang WF, Lau ET, Lam ST, Chan KY, Kan AS, Chau AK, Cheung YF, Lau YL, Chung BH. Liu AP, et al. Among authors: lam st. Eur J Med Genet. 2014 May-Jun;57(6):306-11. doi: 10.1016/j.ejmg.2014.03.014. Epub 2014 Apr 8. Eur J Med Genet. 2014. PMID: 24721633

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. 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

A second report of p.Pro986Leu variant in COL2A1-phenotypic overlap with SEDC and other forms of type II collagenopathies.

Chung BH, Luk HM, Lo IF, Lam ST, Li RH. Chung BH, et al. Among authors: lam st. Am J Med Genet A. 2013 Apr;161A(4):918-20. doi: 10.1002/ajmg.a.35793. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495189 No abstract available.

4

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. 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

5

An analysis of multiple congenital anomaly syndromes in a Chinese population.

Lam ST, Chau AS. Lam ST, et al. Chin Med J (Engl). 1991 Jul;104(7):577-80. Chin Med J (Engl). 1991. PMID: 1831744

6

Genetic services in Hong Kong.

Chau AS, Lam ST, Ghosh A. Chau AS, et al. Among authors: lam st. J Med Genet. 1990 Jun;27(6):380-3. doi: 10.1136/jmg.27.6.380. J Med Genet. 1990. PMID: 2193160 Free PMC article. Review. No abstract available.

7

Macrocephaly-capillary malformation: a report of four Chinese patients and literature review.

Luk HM, Lo IFM, Lai CWS, Yeung WL, Lam STS. Luk HM, et al. Clin Dysmorphol. 2012 Apr;21(2):64-68. doi: 10.1097/MCD.0b013e328350509b. Clin Dysmorphol. 2012. PMID: 22258436 Review.

8

XX-agonadism in a fetus with multiple congenital anomalies.

Woo HH, Lo IF, Tse HY, Lam ST, Tang CH. Woo HH, et al. Among authors: lam st. Am J Med Genet A. 2004 Apr 1;126A(1):104-5. doi: 10.1002/ajmg.a.20554. Am J Med Genet A. 2004. PMID: 15039981 Review.

9

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. Among authors: lam st. Chin Med J (Engl). 2005 Sep 20;118(18):1499-506. Chin Med J (Engl). 2005. PMID: 16232326

10

A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia.

Tsoi H, Yu AC, Chen ZS, Ng NK, Chan AY, Yuen LY, Abrigo JM, Tsang SY, Tsui SK, Tong TM, Lo IF, Lam ST, Mok VC, Wong LK, Ngo JC, Lau KF, Chan TF, Chan HY. Tsoi H, et al. Among authors: lam st. J Med Genet. 2014 Sep;51(9):590-5. doi: 10.1136/jmedgenet-2014-102333. Epub 2014 Jul 25. J Med Genet. 2014. PMID: 25062847 Free PMC 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

130 results

Search Page