Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies

Authors: Pachajoa H, Gomez-Pineda E, Giraldo-Ocampo S, Lores J

Source: Pharmacogenomics and Personalized Medicine, Vol Volume 15, Pp 913-918 (2022)

Subject Terms: neurodevelopmental disorder, zeb2, genetic disorder, multiple congenital disorder, Therapeutics. Pharmacology, RM1-950

File Description: electronic resource

Relation: https://www.dovepress.com/mowat-wilson-syndrome-as-a-differential-diagnosis-in-patients-with-con-peer-reviewed-fulltext-article-PGPM; https://doaj.org/toc/1178-7066

Access URL: https://doaj.org/article/710e3a0da4fa4e15b35048f5cd50a2d2

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