Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Arnold S C, Tan"'
Autor:
Minh Tam Nguyen, Thanh Tung Nguyen, Duy Bac Nguyen, Thi Mai Nguyen, Kim Ngan Nguyen, Van Nhat Minh Ngo, Van Dieu Nguyen, Ngoc Anh Tran, Mulias Lian, Arnold S. C. Tan, Samuel S. Chong, Tien Truong Dang
Publikováno v:
Thrombosis Journal, Vol 21, Iss 1, Pp 1-7 (2023)
Abstract Background Hemophilia A (HEMA) is an X-linked bleeding disorder caused by reduced/absent coagulation factor VIII expression, as a result of pathogenic variants in the F8 gene. Preimplantation prevention of HEMA should ideally include direct
Externí odkaz:
https://doaj.org/article/16b781413ad24e16b88364856c3dd713
Autor:
Min, Chen, Jerry K Y, Chan, Sadhana, Nadarajah, Arnold S C, Tan, Melinda L H, Chan, Joyce, Mathew, Eugene E L, Saw, Cheryl, Lim, Wendy, Wong, Felicia S H, Cheah, Hai-Yang, Law, Peng-Cheang, Wong, Samuel S, Chong
Publikováno v:
Prenatal diagnosis. 35(6)
To develop a single-tube multi-marker assay for improved preimplantation genetic diagnosis (PGD) of deletional and/or non-deletional Hb Bart's hydrops fetalis syndrome, providing haplotype confirmation of deletional status, and maximization of linkag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0190f645f7f17d684869239d2581dcc
https://pubmed.ncbi.nlm.nih.gov/25641621
https://pubmed.ncbi.nlm.nih.gov/25641621
Autor:
Seong Feei, Loh, Peng Cheang, Wong, Boran, Jiang, Gare Hoon, Yeo, Arnold S C, Tan, Ethiraj Balaji, Prasath, Joyce, Mathew, Melinda L H, Chan, Wei Chin, Tan, Mahesh, Choolani, Christine H A, Yap, Samuel S, Chong
Publikováno v:
Singapore medical journal. 53(10)
We aimed to develop and implement a short tandem repeat (STR) polymerase chain reaction alternative to fluorescence in situ hybridisation (FISH) for the preimplantation genetic diagnosis (PGD) of chromosomal translocations.Selected informative STRs l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::10a017316f30629384f0ca17d21b8b7c
https://pubmed.ncbi.nlm.nih.gov/23112015
https://pubmed.ncbi.nlm.nih.gov/23112015
Autor:
Seong Feei Loh, Melinda L. H. Chan, Wei Chin Tan, Ethiraj B. Prasath, Angela Ho, Sherry S.Y. Ho, Boran Jiang, Mui Nee Lim, Arnold S. C. Tan, Joyce Mathew, Gare Hoon Yeo, Mahesh Choolani, Christine Yap, Samuel S. Chong, Peng Cheang Wong, Wen Wang
Publikováno v:
Reproductive biomedicine online. 21(5)
The high incidence of double-gene deletions in α-thalassaemia increases the risk of having pregnancies with homozygous α(0)-thalassaemia, the cause of the lethal haemoglobin (Hb) Bart's hydrops fetalis syndrome. Preimplantation genetic diagnosis (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7dea44ffcd8cc7fed21e9fa1d3dd7ed
https://pubmed.ncbi.nlm.nih.gov/20864413
https://pubmed.ncbi.nlm.nih.gov/20864413
Publikováno v:
Annals of the Academy of Medicine, Singapore. 38(10)
We report the fi rst successful preimplantation genetic diagnosis (PGD) for Hb Bart's hydrops fetalis in Singapore, involving both fresh and frozen embryo replacement cycles.Two couples who were carriers of the Southeast Asian type double gene deleti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::352830827781d327cd0bd5008652794e
https://pubmed.ncbi.nlm.nih.gov/19890585
https://pubmed.ncbi.nlm.nih.gov/19890585
Publikováno v:
Annals of the Academy of Medicine, Singapore. 38(8)
We report on the first successful preimplantation genetic diagnosis (PGD) in Singapore.A couple who are beta-thalassaemia carriers and have an affected daughter requested for PGD.Two cycles of PGD were performed on the couple. Beta-thalassaemia mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5972929d85bb4b1406af1ee2e0bec08e
https://pubmed.ncbi.nlm.nih.gov/19736578
https://pubmed.ncbi.nlm.nih.gov/19736578
Autor:
Le Ye, Lee, Swee Chye, Quek, Samuel S, Chong, Arnold S C, Tan, Josephine M S, Lum, Denise Li-Meng, Goh
Publikováno v:
Annals of the Academy of Medicine, Singapore. 35(12)
Williams syndrome (WS) is a rare but well recognised neurodevelopmental disease affecting the connective tissue and the central nervous system. Many patients are identified through the presence of dysmorphic features and associated cardiac abnormalit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15490163f0fa0942b83a5d3fc01b6a4d
https://pubmed.ncbi.nlm.nih.gov/17219004
https://pubmed.ncbi.nlm.nih.gov/17219004
Publikováno v:
Clinical chemistry. 48(6 Pt 1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::28f39cb726a552cb41f275231c988e4a
https://pubmed.ncbi.nlm.nih.gov/12029018
https://pubmed.ncbi.nlm.nih.gov/12029018