Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Felicia S H, Cheah"'
Publikováno v:
PLoS ONE, Vol 12, Iss 7, p e0180984 (2017)
Molecular diagnosis of Huntington disease (HD) is currently performed by fluorescent repeat-flanking or triplet-primed PCR (TP-PCR) with capillary electrophoresis (CE). However, CE requires multiple post-PCR steps and may result in high cost in high-
Externí odkaz:
https://doaj.org/article/153914eea7724dd8aa2e44114a9685dd
Autor:
Qianqian Chen, Hong Wang, Jacqueline B Hetmanski, Tianxiao Zhang, Ingo Ruczinski, Holger Schwender, Kung Yee Liang, M Daniele Fallin, Richard J Redett, Gerald V Raymond, Yah-Huei Wu Chou, Philip Kuo-Ting Chen, Vincent Yeow, Samuel S Chong, Felicia S H Cheah, Ethylin Wang Jabs, Alan F Scott, Terri H Beaty
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e35347 (2012)
The Bone Morphogenetic Protein 4 gene (BMP4) is located in chromosome 14q22-q23 which has shown evidence of linkage for isolated nonsyndromic cleft lip with or without cleft palate (NSCL/P) in a genome wide linkage analysis of human multiplex familie
Externí odkaz:
https://doaj.org/article/8afa1708bd2c4ecfbf85f443208ad079
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
Autor:
Zhao, Mingjue1, Cheah, Felicia S. H.2, Chen, Min1, Lee, Caroline G.3,4,5, Law, Hai-Yang6, Chong, Samuel S.1,2,7
Publikováno v:
PLoS ONE. 7/10/2017, Vol. 12 Issue 7, p1-17. 17p.
Autor:
Chen, Min, Chan, Jerry K. Y., Nadarajah, Sadhana, Tan, Arnold S. C., Chan, Melinda L. H., Mathew, Joyce, Saw, Eugene E. L., Lim, Cheryl, Wong, Wendy, Cheah, Felicia S. H., Law, Hai‐Yang, Wong, Peng‐Cheang, Chong, Samuel S.
Publikováno v:
Prenatal Diagnosis; Jun2015, Vol. 35 Issue 6, p534-543, 10p
Autor:
Gare Hoon Yeo, Cheah, Felicia S. H., Winkler, Christoph, Jabs, Ethylin Wang, Venkatesh, Byrappa, Chong, Samuel S.
Publikováno v:
Development Genes & Evolution; Jun2009, Vol. 219 Issue 6, p289-300, 12p, 4 Color Photographs, 2 Diagrams, 1 Chart, 1 Graph
Publikováno v:
Development Genes & Evolution; Nov/Dec2007, Vol. 217 Issue 11/12, p783-789, 7p, 4 Diagrams, 3 Charts
Autor:
Nicoli, Paolo, Calabrese, Chiara, Pellegrino, Rosa Maria, Rosso, Valentina, Bracco, Enrico, Signorino, Elisabetta, Carturan, Sonia, Petiti, Jessica, Gallo, Daniela, Gaidano, Valentina, De Gobbi, Marco, Roetto, Antonella, Saglio, Giuseppe, Cilloni, Daniela
Publikováno v:
American Journal of Hematology; Sep2015, Vol. 90 Issue 9, pE193-E194, 2p
Autor:
Chen, Min, Loh, Seong Feei, Yu, Su Ling, Nair, Suresh, Tan, Heng Hao, Nadarajah, Sadhana, Wong, Peng-Cheang, Ng, Soon Chye, Prasath, Ethiraj B., Tan, Arnold S.C., Cheah, Felicia S.H., Saw, Eugene E.L., Chong, Samuel S.
Publikováno v:
American Journal of Hematology; Sep2015, Vol. 90 Issue 9, pE194-E196, 1p
Autor:
Diego F. Wyszynski
Majoradvances in the diagnosis and treatment of oral clefts have been made in the past 50 years, and recent genetics and epidemiological studies have led to new theories about the causes of cleft lip and palate. Addressing issues that are relevant to