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Author/Creator Foo, Roger

3. Characterization of CaV1.2 exon 33 heterozygous knockout mice and negative correlation between Rbfox1 and CaV1.2 exon 33 expressions in human heart failure. Issue 1 (1st January 2018)

Authors:
Wang, Juejin; Li, Guang; Yu, Dejie; Wong, Yuk Peng; Yong, Tan Fong; Liang, Mui Cheng; Liao, Ping; Foo, Roger; Hoppe, Uta C.; Soong, Tuck Wah
Journal:
Channels
Issue:
Volume 12:Issue 1(2018)
Page Start:
51
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Correction: Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders. (December 2018)

Authors:
Bylstra, Yasmin; Kuan, Jyn; Lim, Weng; Bhalshankar, Jaydutt; Teo, Jing; Davila, Sonia; Teh, Bin; Rozen, Steve; Tan, Ene-Choo; Liew, Wendy; Yeo, Khung; Tan, Patrick; Saw, Seang; Cheng, Ching-Yu; Cook, Stuart; Foo, Roger; Jamuar, Saumya
Journal:
Genetics in medicine
Issue:
Volume 20:Number 12(2018)
Page Start:
1692
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

8. PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. Issue 2 (2nd November 2017)

Authors:
Reijnders, Margot R F; Janowski, Robert; Alvi, Mohsan; Self, Jay E; van Essen, Ton J; Vreeburg, Maaike; Rouhl, Rob P W; Stevens, Servi J C; Stegmann, Alexander P A; Schieving, Jolanda; Pfundt, Rolph; van Dijk, Katinke; Smeets, Eric; Stumpel, Connie T R M; Bok, Levinus A; Cobben, Jan Maarten; Enge...
Journal:
Journal of medical genetics
Issue:
Volume 55:Issue 2(2018)
Page Start:
104
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗