Complexities of Clinical Genetics Consultation: An Interprofessional Clinical Skills Workshop

por Hoffman, Jodi D., Thompson, Rachel, Swenson, Kathleen B., Dasgupta, Shoumita
Publicado 2020

Neonatal arrhythmias in Turner syndrome: a case report and review of the literature

por Choi, Yeyoon, Hoffman, Jodi, Alarcon, Lizzeth, Pfau, Jennifer, Bolourchi, Meena
Publicado 2021

OTX2 Duplication Is Implicated in Hemifacial Microsomia

por Zielinski, Dina, Markus, Barak, Sheikh, Mona, Gymrek, Melissa, Chu, Clement, Zaks, Marta, Srinivasan, Balaji, Hoffman, Jodi D., Aizenbud, Dror, Erlich, Yaniv
Publicado 2014

Next-generation DNA sequencing of HEXA: a step in the right direction for carrier screening

por Hoffman, Jodi D, Greger, Valerie, Strovel, Erin T, Blitzer, Miriam G, Umbarger, Mark A, Kennedy, Caleb, Bishop, Brian, Saunders, Patrick, Porreca, Gregory J, Schienda, Jaclyn, Davie, Jocelyn, Hallam, Stephanie, Towne, Charles
Publicado 2013

Evaluation and classification of severity for 176 genes on an expanded carrier screening panel

por Arjunan, Aishwarya, Bellerose, Holly, Torres, Raul, Ben‐Shachar, Rotem, Hoffman, Jodi D., Angle, Brad, Slotnick, Robert Nathan, Simpson, Brittany N., Lewis, Andrea M., Magoulas, Pilar L., Bontempo, Kelly, Schulze, Jeanine, Tarpinian, Jennifer, Bucher, Jessica A., Dineen, Richard, Goetsch, Allison, Lazarin, Gabriel A., Johansen Taber, Katherine
Publicado 2020