Developmental delay, coarse facial features, and epilepsy in a patient with EXT2 gene variants

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Bibliographic Details
Published inClinical case reports Vol. 7; no. 4; pp. 632 - 637
Main Authors Gupta, Aditi, Ewing, Sarah A, Renaud, Deborah L, Hasadsri, Linda, Raymond, Kimiyo M, Klee, Eric W, Gavrilova, Ralitza H
Format Report
LanguageEnglish
Published 01.04.2019
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Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:2050-0904
2050-0904
DOI:10.1002/ccr3.2010