Una revisión actualizada del síndrome de deleción (monosomía) 1p36
Abstract
The Monosomy 1p36 deletion syndrome is part of the group of diseases known as Rare Diseases. The objective of the present work is to review the characteristics of Monosomy 1p36 deletion syndrome. The monosomy 1p36 deletion syndrome phenotype includes: dysmorphic craniofacial features; large anterior fontanelle, unibrow, deep-set eyes, epicanthus, wide nasal root/bridge, mandible hypoplasia, abnormal location of the pinna, philtrum and pointed...
Paper Details
Title
Una revisión actualizada del síndrome de deleción (monosomía) 1p36
Published Date
Sep 1, 2016
Volume
87
Issue
5
Pages
411 - 421
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