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1. A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype. Issue 9 (28th May 2014)

3. Cover. Issue 2 (7th February 2020)

4. Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi‐Ethnic Allele and Copy Number Variant Detection. Issue 1 (5th August 2020)

6. Integrated CYP2D6 interrogation for multiethnic copy number and tandem allele detection. (6th December 2018)

7. Lessons learned from expanded reproductive carrier screening in self‐reported Ashkenazi, Sephardi, and Mizrahi Jewish patients. Issue 2 (27th December 2019)