Open AccessMowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies
Author(s) -
Harry Pachajoa,
E. Gómez-Pineda,
Sebastián Giraldo-Ocampo,
Juliana Lores
Publication year - 2022
Publication title -
pharmacogenomics and personalized medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.845
H-Index - 28
ISSN - 1178-7066
DOI - 10.2147/pgpm.s380908
Subject(s) - medicine , microcephaly , intellectual disability , pediatrics , nonsense , facial dysmorphism , genetic disorder , heart defect , heart disease , psychiatry , genetics , pathology , gene , disease , biology , phenotype
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