Chan YM - Search Results

1

Chinese women's preferences for prenatal diagnostic procedure and their willingness to trade between procedures.

Chan YM, Sahota DS, Leung TY, Choy KW, Chan OK, Lau TK. Chan YM, et al. Among authors: chan ok. Prenat Diagn. 2009 Dec;29(13):1270-6. doi: 10.1002/pd.2394. Prenat Diagn. 2009. PMID: 19862769

2

The utility assessment of Chinese pregnant women towards the birth of a baby with Down syndrome compared to a procedure-related miscarriage.

Chan YM, Leung TN, Leung TY, Fung TY, Chan LW, Lau TK. Chan YM, et al. Among authors: chan lw. Prenat Diagn. 2006 Sep;26(9):819-24. doi: 10.1002/pd.1511. Prenat Diagn. 2006. PMID: 16832829

3

Miscarriage after invasive prenatal diagnostic procedures: how much risk our pregnant women are willing to take?

Chan YM, Sahota DS, Chan OK, Leung TY, Lau TK. Chan YM, et al. Among authors: chan ok. Prenat Diagn. 2009 Sep;29(9):870-4. doi: 10.1002/pd.2305. Prenat Diagn. 2009. PMID: 19499531

4

Patient's choice between a non-invasive prenatal test and invasive prenatal diagnosis based on test accuracy.

Chan YM, Leung TY, Chan OK, Cheng YK, Sahota DS. Chan YM, et al. Among authors: chan ok. Fetal Diagn Ther. 2014;35(3):193-8. doi: 10.1159/000356075. Epub 2013 Nov 13. Fetal Diagn Ther. 2014. PMID: 24247224

5

Women's uptake of non-invasive DNA testing following a high-risk screening test for trisomy 21 within a publicly funded healthcare system: findings from a retrospective review.

Chan YM, Leung WC, Chan WP, Leung TY, Cheng YK, Sahota DS. Chan YM, et al. Among authors: chan wp. Prenat Diagn. 2015 Apr;35(4):342-7. doi: 10.1002/pd.4544. Epub 2015 Jan 4. Prenat Diagn. 2015. PMID: 25484032

6

Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction.

Kong GW, Cao Y, Huang J, Cheng KY, Pursley AN, Rosenfeld JA, Edwards JG, Chan YM, Cheung SW, Leung TY, Choy KW. Kong GW, et al. Among authors: chan ym. Prenat Diagn. 2016 Dec;36(13):1211-1216. doi: 10.1002/pd.4959. Epub 2016 Nov 29. Prenat Diagn. 2016. PMID: 27859473

7

Prenatal diagnosis of maternally inherited X-linked Opitz G/BBB syndrome by chromosomal microarray in a fetus with complex congenital heart disease.

Cheng YK, Huang J, Law KM, Chan YM, Leung TY, Choy KW. Cheng YK, et al. Among authors: chan ym. Clin Chim Acta. 2014 Sep 25;436:140-2. doi: 10.1016/j.cca.2014.05.006. Epub 2014 May 23. Clin Chim Acta. 2014. PMID: 24863803

8

Acceptance towards giving birth to a child with beta-thalassemia major - A prospective study.

Chan YM, Chan OK, Cheng YKY, Leung TY, Lao TTH, Sahota DS. Chan YM, et al. Among authors: chan ok. Taiwan J Obstet Gynecol. 2017 Oct;56(5):618-621. doi: 10.1016/j.tjog.2017.08.007. Taiwan J Obstet Gynecol. 2017. PMID: 29037546 Free article.

9

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.

Chau MHK, Cao Y, Kwok YKY, Chan S, Chan YM, Wang H, Yang Z, Wong HK, Leung TY, Choy KW. Chau MHK, et al. Among authors: chan s, chan ym. Am J Obstet Gynecol. 2019 Nov;221(5):493.e1-493.e11. doi: 10.1016/j.ajog.2019.06.007. Epub 2019 Jun 14. Am J Obstet Gynecol. 2019. PMID: 31207233

10

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.

Hui AS, Chau MHK, Chan YM, Cao Y, Kwan AH, Zhu X, Kwok YK, Chen Z, Lao TT, Choy KW, Leung TY. Hui AS, et al. Among authors: chan ym. Acta Obstet Gynecol Scand. 2021 Feb;100(2):235-243. doi: 10.1111/aogs.14003. Epub 2020 Oct 15. Acta Obstet Gynecol Scand. 2021. PMID: 32981064 Free article.

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