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You searched for: Author/Creator Cheah, Felicia S.H.

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1. FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome. (19th July 2017)

2. Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay. Issue 9 (14th August 2015)

4. The FGF and FGFR Gene Family and Risk of Cleft Lip with or Without Cleft Palate. (January 2013)