Lau ET - Search Results

1

Semi-quantitative fluorescent PCR analysis identifies PRKAA1 on chromosome 5 as a potential candidate cancer gene of cervical cancer.

Huang FY, Chiu PM, Tam KF, Kwok YK, Lau ET, Tang MH, Ng TY, Liu VW, Cheung AN, Ngan HY. Huang FY, et al. Among authors: lau et. Gynecol Oncol. 2006 Oct;103(1):219-25. doi: 10.1016/j.ygyno.2006.02.028. Epub 2006 Apr 3. Gynecol Oncol. 2006. PMID: 16595147

2

Genetic abnormalities and HPV status in cervical and vulvar squamous cell carcinomas.

Huang FY, Kwok YK, Lau ET, Tang MH, Ng TY, Ngan HY. Huang FY, et al. Among authors: lau et. Cancer Genet Cytogenet. 2005 Feb;157(1):42-8. doi: 10.1016/j.cancergencyto.2004.06.002. Cancer Genet Cytogenet. 2005. PMID: 15676146

3

Maternal plasma or human serum albumin in wash buffer enhances enrichment and ex vivo expansion of human umbilical cord blood CD34+ cells.

Kwok YK, Tang MH, Law HK, Ngai CS, Lau YL, Lau ET. Kwok YK, et al. Among authors: lau et, lau yl. Br J Haematol. 2007 Jun;137(5):468-74. doi: 10.1111/j.1365-2141.2007.06606.x. Br J Haematol. 2007. PMID: 17488490 Free article.

4

Prenatal detection of a de novo Yqh-acrocentric translocation.

Ng LK, Kwok YK, Tang LY, Ng PP, Ghosh A, Lau ET, Tang MH. Ng LK, et al. Among authors: lau et. Clin Biochem. 2006 Mar;39(3):219-23. doi: 10.1016/j.clinbiochem.2006.01.013. Epub 2006 Mar 3. Clin Biochem. 2006. PMID: 16515778

5

Rapid aneuploidy screening (FISH or QF-PCR): the changing scene in prenatal diagnosis?

Leung WC, Lau ET, Lao TT, Tang MH. Leung WC, et al. Among authors: lau et. Expert Rev Mol Diagn. 2004 May;4(3):333-7. doi: 10.1586/14737159.4.3.333. Expert Rev Mol Diagn. 2004. PMID: 15137900 Review.

6

Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood.

Lau ET, Kwok YK, Luo HY, Leung KY, Lee CP, Lam YH, Chui DH, Tang MH. Lau ET, et al. Prenat Diagn. 2005 Feb;25(2):123-8. doi: 10.1002/pd.1096. Prenat Diagn. 2005. PMID: 15712347

7

Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures.

Lau ET, Kwok YK, Chui DH, Wong HS, Luo HY, Tang MH. Lau ET, et al. Prenat Diagn. 2001 Jul;21(7):529-39. doi: 10.1002/pd.81. Prenat Diagn. 2001. PMID: 11494285

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. Among authors: lau et. 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

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: lau et. 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

10

A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16.

Au PK, Kan AS, Tang MH, Leung KY, Chan KY, Tang TW, Lau ET. Au PK, et al. Among authors: lau et. Hemoglobin. 2016;40(1):66-9. doi: 10.3109/03630269.2015.1096283. Epub 2015 Nov 16. Hemoglobin. 2016. PMID: 26574185

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