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2. Generation of reporter hESCs by targeting EGFP at the CD144 locus to facilitate the endothelial differentiation. (25th April 2018)

4. Prenatal case of Simpson–Golabi–Behmel syndrome with a de novo 370Kb‐sized microdeletion of Xq26.2 compassing partial GPC3 gene and review. Issue 8 (22nd July 2021)

5. Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family. Issue 3 (20th January 2021)