Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease)

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Bibliographic Details
Published in:Journal of pediatric genetics 2018, Vol.7 (3), p.134-137
Main Authors: Costain, Gregory, Inbar-Feigenberg, Michal, Saleh, Maha, Yaniv-Salem, Shimrit, Ryan, Greg, Morgen, Eric, Goh, Elaine S, Nishimura, Gen, Chitayat, David
Format: Report
Language:English
Online Access:Get full text
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ISSN:2146-4596
DOI:10.1055/s-0038-1636995