Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pui Shan Salome Lo"'
Autor:
Mei Ki Chan, Tsz Kin Lo, Kwong Wai Choy, Pui Shan Salome Lo, Hongyun Zhang, Wei Wang, Tze Kin Lau, Fang Chen, Fu Man Jiang, Robert J. Stevenson, Lin Wai Chan
Publikováno v:
Prenatal Diagnosis. 33:602-608
Objective To report secondary or additional findings arising from introduction of non-invasive prenatal testing (NIPT) for aneuploidy by whole genome sequencing as a clinical service. Methods Five cases with secondary findings were reviewed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02180831c2cfda4e203ed24546d5d1a1
https://doi.org/10.1002/pd.4076
https://doi.org/10.1002/pd.4076
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 26:434-437
Non-invasive prenatal screening for fetal Down syndrome (NIFTY) by maternal plasma sequencing was performed in 12 subjects with twin pregnancies, including 11 with normal fetuses and 1 with discordant fetal Trisomy 21. For every sample, it was proces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d590582447af26207cacdf55ceac890
https://doi.org/10.3109/14767058.2012.733768
https://doi.org/10.3109/14767058.2012.733768
Autor:
Tik Yee Koo, Tze Kin Lau, Mei Ki Chan, Pui Shan Salome Lo, Waisze Kim Chan, Hoi Yan Joyce Ng, Ritsuko K Pooh, Hon Yee Connie Chan
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 25:2616-2619
To study whether pregnant women would like to be informed if sex chromosomal abnormalities (SCA) were suspected with the non-invasive prenatal diagnosis of fetal Down syndrome (the NIFTY) test.Two hundred and one patients carried a singleton pregnanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df753758a7f3db1911f12c405192f7df
https://doi.org/10.3109/14767058.2012.712569
https://doi.org/10.3109/14767058.2012.712569
Autor:
H. Choi, Tze Kin Lau, Lei Zhang, Mei Ki Chan, Wei Wang, Pui Shan Salome Lo, Fang Chen, Fuman Jiang, Hongyun Zhang
Publikováno v:
Prenatal Diagnosis. 33:198-200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8cd1f2b841c665119dbf0bad6c9c401
https://doi.org/10.1002/pd.4024
https://doi.org/10.1002/pd.4024
Autor:
Tze Kin, Lau, Fu Man, Jiang, Robert J, Stevenson, Tsz Kin, Lo, Lin Wai, Chan, Mei Ki, Chan, Pui Shan Salome, Lo, Wei, Wang, Hong-Yun, Zhang, Fang, Chen, Kwong Wai, Choy
Publikováno v:
Prenatal diagnosis. 33(6)
To report secondary or additional findings arising from introduction of non-invasive prenatal testing (NIPT) for aneuploidy by whole genome sequencing as a clinical service.Five cases with secondary findings were reviewed.In Case 1, NIPT revealed a l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5058961a91d1a592206e2841ec03296
https://pubmed.ncbi.nlm.nih.gov/23553438
https://pubmed.ncbi.nlm.nih.gov/23553438
Autor:
Tik Yee Koo, Pui Shan Salome Lo, Wai Sze Kim Chan, Mei Ki Chan, Hoi Yan Joyce Ng, Ritsuko K Pooh, Tze Kin Lau, Hon Yee Connie Chan
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine
Objective: To report the initial experience of noninvasive prenatal diagnosis of fetal Down syndrome (The NIFTY test) in a clinical setting. Methods: The NIFTY test was offered as a screening test for fetal Down syndrome to pregnant women with a sing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ae47ef719fe2e08620e6222b3fe99fc
https://pubmed.ncbi.nlm.nih.gov/22471583
https://pubmed.ncbi.nlm.nih.gov/22471583