A commentary on de novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux

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Bibliographic Details
Published in:Journal of human genetics 2016-09, Vol.61 (9), p.773-774
Main Authors: Takai, Rie, Ohta, Tohru
Format: Article
Language:English
Subjects:
Developmental Disabilities - diagnosis
Developmental Disabilities - genetics
Gastroesophageal Reflux - diagnosis
Gastroesophageal Reflux - genetics
Genetic Association Studies
Homeodomain Proteins - genetics
Humans
Mutation
Syndrome
Transcription Factors - genetics
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ISSN:1434-5161
1435-232X
DOI:10.1038/jhg.2016.81