Alex R Paciorkowski

Years Active: 2017-2017
Publications (10 Years): 2

This page only lists publications with an associated author ORCID identifier.

Publications

Kaylee Park, Laurie E Seltzer, Emily Tuttle, Ghayda M Mirzaa, Alex R Paciorkowski
PLXNA1 developmental encephalopathy with syndromic features: A case report and review of the literature. American journal of medical genetics. Part A 173 (7) (2017)
Bo Hoon Lee, Margot R F Reijnders, Oluwatobi Abubakare, Emily Tuttle, Brynn Lape, Kelly Q Minks, Christopher Stodgell, Loisa Bennetto, Jennifer Kwon, Chin-To Fong, Karen W Gripp, Eric D Marsh, Wendy E Smith, Ahm M Huq, Stephanie A Coury, Wen-Hann Tan, Orestes Solis, Rupal I Mehta, Richard J Leventer, Diana Baralle, David Hunt, Alex R Paciorkowski
Expanding the neurodevelopmental phenotype of PURA syndrome. American journal of medical genetics. Part A 176 (1) (2017)

Alex R Paciorkowski.css-eqlu8i{font-size:small;padding-left:4px;}