Zobrazeno 1 - 3
of 3
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