The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

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Bibliographic Details
Published in:The Turkish journal of pediatrics Vol. 61; no. 4; pp. 589 - 593
Main Authors: Gürsoy, Semra, Kutbay, Yaşar Bekir, Özdemir, Taha Reşid, Hazan, Filiz
Format: Report
Language:English
Published: 01-01-2019
Online Access:Get full text
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Description
Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:0041-4301
DOI:10.24953/turkjped.2019.04.017