Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Yuen-Ming Tan"'
Autor:
Nikki Fong, Jiin Ying Lim, Breana Cham, Sylvia Kam, Chew Yin Goh, Heming Wei, Yuen Ming Tan, Hai Yang Law, Weng Khong Lim, Ee Shien Tan, Ene Choo Tan, Saumya Shekhar Jamuar
Publikováno v:
Annals of the Academy of Medicine, Singapore. 51(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2a657c195b364d89ec03db9342c5028
https://pubmed.ncbi.nlm.nih.gov/36592150
https://pubmed.ncbi.nlm.nih.gov/36592150
Autor:
Breana Cham, Jiin Ying Lim, Wendy K.M. Liew, Yuen-Ming Tan, Jyn-Ling Kuan, Bruno Reversades, Raman Sethi, Alvin Yu Jin Ng, Nathalie Escande-Beillard, Alexander Lezhava, Sumanty Tohari, Heming Wei, Arun George Devasia, Deepa Subramanian, Sylvia Kam, Woei Kang Liew, Min Xie, Kanika Jain, Saumya Shekhar Jamuar, Hai-Yang Law, Ee Shien Tan, Nilesh R. Tawari, Swati Tomar, Ene-Choo Tan, Ivy Ng, Carine Bonnard, Grace Lin, Angeline Lai, Chew Yin Jasmine Goh, Perumal Dharuman, Poh San Lai, Arthi Shanmugasundaram, Huilin Chin, Neha Singh Bhatia, Denise L.M. Goh, Maggie Brett, Célia Bosso-Lefèvre, Grace K. Tan, Teck Wah Ting, Roger Foo, Sarah B Ng, Cheuk Ka Tong, Byrappa Venkatesh, Zenia Tiang
Publikováno v:
Archives of Disease in Childhood. 106:31-37
ObjectiveUse next-generation sequencing (NGS) technology to improve our diagnostic yield in patients with suspected genetic disorders in the Asian setting.DesignA diagnostic study conducted between 2014 and 2019 (and ongoing) under the Singapore Undi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9bba7015302a03439efc4b46889a6c9
https://doi.org/10.1136/archdischild-2020-319180
https://doi.org/10.1136/archdischild-2020-319180
Autor:
Yanqun Liu, Min Hoe Chew, Xue Wei Goh, Soo Yong Tan, Carol Tien Tau Loi, Yuen Ming Tan, Hai Yang Law, Poh Koon Koh, Choong Leong Tang
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94170 (2014)
BACKGROUND: Germline defects of mismatch repair (MMR) genes underlie Lynch Syndrome (LS). We aimed to gain comprehensive genetic and epigenetic profiles of LS families in Singapore, which will facilitate efficient molecular diagnosis of LS in Singapo
Externí odkaz:
https://doaj.org/article/93367982a34f4c27b632e9fb511a869d
Autor:
Yuen Ming Tan, Wendy Low, Hui Jing Ee, Weng Khong Lim, Ene-Choo Tan, Jiin Ying Lim, Angeline Lai, Juin Yee Kong, Teck Wah Ting, Hai-Yang Law, Ivy Ng, Nikki Fong, Ee Shien Tan, Ai Ling Koh, Chew Yin Jasmine Goh, Jyn Ling Kuan, Saumya Shekhar Jamuar, Heming Wei, Sylvia Kam, Leng Kee Ching, Breana Cham, Lik Eng Loh
Objective: Use rapid next-generation sequencing (NGS) to improve our diagnostic yield in critically ill paediatric patients with suspected genetic disorders in the Asian setting.Design: A diagnostic study conducted between April 2018 and January 2019
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::129c65a6a236ebe7e845df4928c37b44
https://doi.org/10.21203/rs.3.rs-384663/v1
https://doi.org/10.21203/rs.3.rs-384663/v1
Publikováno v:
Annals of Translational Medicine. 5:AB091-AB091
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8279c7d8d5435962cbbee2946e180c6f
https://doi.org/10.21037/atm.2017.s091
https://doi.org/10.21037/atm.2017.s091
Autor:
Yuen Ming Tan, Min Hoe Chew, Hai-Yang Law, Xue Wei Goh, Poh Koon Koh, Yanqun Liu, Carol Loi, Soo Yong Tan, Choong Leong Tang
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 4, p e94170 (2014)
PLoS ONE, Vol 9, Iss 4, p e94170 (2014)
Background Germline defects of mismatch repair (MMR) genes underlie Lynch Syndrome (LS). We aimed to gain comprehensive genetic and epigenetic profiles of LS families in Singapore, which will facilitate efficient molecular diagnosis of LS in Singapor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8019294dd31d2fe07175fc93ba6ab5fb
http://europepmc.org/articles/PMC3978005
http://europepmc.org/articles/PMC3978005
Publikováno v:
Analytical biochemistry. 404(1)
Based on a novel Q-primer real-time polymerase chain reaction (PCR) system, we designed allele-specific Q-primers for the detection of three β-thalassemia mutations [Cd41/42(-TCTT), IVSI nt5 (G>C), and IVSII nt654 (C>T)] that have a high carrier fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33277e791898290ac3068ccca2b7156
https://pubmed.ncbi.nlm.nih.gov/20433808
https://pubmed.ncbi.nlm.nih.gov/20433808
Autor:
Yuen-Ming Tan, Kah-Yin Loke
Publikováno v:
Diagnostic molecular pathology : the American journal of surgical pathology, part B. 14(4)
The short stature homeobox-containing (SHOX) gene, found on the human sex chromosomes, has a role in bone growth and height determination. Haploinsufficiency of the SHOX gene is believed to be responsible for poor growth such as that observed in ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde3424d2dcb16840fee6f16560ac0a6
https://pubmed.ncbi.nlm.nih.gov/16319696
https://pubmed.ncbi.nlm.nih.gov/16319696
Publikováno v:
Clinical Dysmorphology. 17:73-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e19f5f405984a68a628e779649d7bf2
https://doi.org/10.1097/mcd.0b013e3282efdaf1
https://doi.org/10.1097/mcd.0b013e3282efdaf1