Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sherry S Y, Ho"'
Autor:
Angela N. Barrett, Zhouwei Huang, Sarah Aung, Sherry S. Y. Ho, Nur Syazana Roslan, Aniza P. Mahyuddin, Arijit Biswas, Mahesh Choolani
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2257
The current gold standard for the definitive diagnosis of fetal aneuploidy uses either chorionic villus sampling (CVS) or amniocentesis, both of which are which are invasive procedures carrying a procedure-related risk of miscarriage of up to 0.1–0
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33124076020fdcdbfaa0b207b45f68bb
https://doi.org/10.3390/genes13122257
https://doi.org/10.3390/genes13122257
Autor:
Aniza Puteri Mahyuddin, Huang Zhouwei, Rui Hua, Song Quan, Mahesh Choolani, Sukumar Ponnusamy, Jaspal Singh Sandhu, Jerry Kok Yen Chan, Angela N. Barrett, Sherry S. Y. Ho, Samuel S. Chong, Tuan Zea Tan
Publikováno v:
Prenatal Diagnosis. 35:637-644
Objective The objective of the study was to detect aneuploidy in single fetal nucleated red blood cells (FNRBCs) from placental villi using whole genome amplification (WGA) and next generation sequencing. Methods Three single FNRBCs per sample were m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::879ff0bb84ea6d37cf041ee48d91b28c
https://doi.org/10.1002/pd.4491
https://doi.org/10.1002/pd.4491
Autor:
Sherry S. Y. Ho, Mahesh Choolani, Evelyn Siew-Chuan Koay, Leena Gole, Arijit Biswas, Cuiwen Chua
Publikováno v:
Prenatal Diagnosis. 32:321-328
Rapid molecular prenatal diagnostic methods, such as fluorescence in situ hybridization (FISH), quantitative fluorescence-PCR, and multiplex ligation-dependent probe amplification, can detect common fetal aneuploidies within 24 to 48 h. However, spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81b5108f3bb55734eb0396fd1150edb3
https://doi.org/10.1002/pd.2946
https://doi.org/10.1002/pd.2946
Autor:
Samuel S. Chong, Arijit Biswas, Sonia Baig, Jerry Chan, Mary Rauff, Lily Chiu, Yiong Huak Chan, Mahesh Choolani, Sukumar Ponnusamy, Evelyn Siew-Chuan Koay, Sinuhe Hahn, Lin Lin Su, Sherry S. Y. Ho
Publikováno v:
Prenatal Diagnosis. 30:65-73
Objective Prenatal diagnosis of alpha-thalassaemia requires invasive testing associated with a risk of miscarriage. Cell-free foetal DNA in maternal plasma presents an alternative source of foetal genetic material for noninvasive prenatal diagnosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a637eda0675f53ab1c440d872e51538
https://doi.org/10.1002/pd.2413
https://doi.org/10.1002/pd.2413
Autor:
Rui, Hua, Angela N, Barrett, Tuan Zea, Tan, Zhouwei, Huang, Aniza Puteri, Mahyuddin, Sukumar, Ponnusamy, Jaspal Singh, Sandhu, Sherry S Y, Ho, Jerry K Y, Chan, Samuel, Chong, Song, Quan, Mahesh, Choolani
Publikováno v:
Prenatal diagnosis. 35(7)
The objective of the study was to detect aneuploidy in single fetal nucleated red blood cells (FNRBCs) from placental villi using whole genome amplification (WGA) and next generation sequencing.Three single FNRBCs per sample were manually picked from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b2c5a6a4e6b3932bc78fc851fcc8eed
https://pubmed.ncbi.nlm.nih.gov/25178640
https://pubmed.ncbi.nlm.nih.gov/25178640
Autor:
Sherry S Y, Ho, Mahesh A, Choolani
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 659
Fluorescence in situ hybridization (FISH) and quantitative fluorescence (QF)-PCR are rapid molecular methods that test for common chromosomal aneuploidies in prenatal diagnosis. While cytogenetic analysis requires approximately 7-14 days before fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6005b33d4ddfff3f21eda8a9627621f3
https://pubmed.ncbi.nlm.nih.gov/20809318
https://pubmed.ncbi.nlm.nih.gov/20809318
Autor:
Sherry S. Y. Ho, Mahesh Choolani
Publikováno v:
Methods in Molecular Biology ISBN: 9781607617884
Fluorescence in situ hybridization (FISH) and quantitative fluorescence (QF)-PCR are rapid molecular methods that test for common chromosomal aneuploidies in prenatal diagnosis. While cytogenetic analysis requires approximately 7-14 days before fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8104ae950e7cd9185f6bbc53668f923
https://doi.org/10.1007/978-1-60761-789-1_19
https://doi.org/10.1007/978-1-60761-789-1_19
Autor:
Barrett, Angela N., Huang, Zhouwei, Aung, Sarah, Ho, Sherry S. Y., Roslan, Nur Syazana, Mahyuddin, Aniza P., Biswas, Arijit, Choolani, Mahesh
Publikováno v:
Genes; Dec2022, Vol. 13 Issue 12, p2257, 9p
Autor:
Ho, Sherry S. Y., Choolani, Mahesh A.
Publikováno v:
Fluorescence in Situ Hybridization (FISH); 2010, p261-268, 8p
Autor:
Hua, Rui, Barrett, Angela N., Tan, Tuan Zea, Huang, Zhouwei, Mahyuddin, Aniza Puteri, Ponnusamy, Sukumar, Sandhu, Jaspal Singh, Ho, Sherry S. Y., Chan, Jerry K. Y., Chong, Samuel, Quan, Song, Choolani, Mahesh
Publikováno v:
Prenatal Diagnosis; Jul2015, Vol. 35 Issue 7, p637-644, 8p