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Author/Creator Qian, Emily

2. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. Issue 1 (8th October 2021)

Authors:
Werner, Kelly M.; Cox, Allison J.; Qian, Emily; Jain, Preti; Ji, Weizhen; Tikhonova, Irina; Castaldi, Christopher; Bilguvar, Kaya; Knight, James; Ferdinandusse, Sacha; Fawaz, Rima; Jiang, Yong‐Hui; Gallagher, Patrick G.; Bizzarro, Matthew; Gruen, Jeffrey R.; Bale, Allen; Zhang, Hui
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 1(2022)
Page Start:
357
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Elective genomic testing: Practice resource of the National Society of Genetic Counselors. Issue 2 (4th January 2023)

Authors:
Blout Zawatsky, Carrie L.; Bick, David; Bier, Louise; Funke, Birgit; Lebo, Matthew; Lewis, Katie L.; Orlova, Ekaterina; Qian, Emily; Ryan, Lauren; Schwartz, Marci L. B.; Soper, Emily R.
Journal:
Journal of genetic counseling
Issue:
Volume 32:Issue 2(2023)
Page Start:
281
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗