A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features

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Bibliographic Details
Main Authors: Vinkler, Chana (Author) , Haas, Dorothea (Author)
Format: Article (Journal)
Language:English
Published: 2014
In: European journal of medical genetics
Year: 2014, Volume: 57, Issue: 6, Pages: 288-292
ISSN:1878-0849
DOI:10.1016/j.ejmg.2014.03.010
Online Access:Verlag, Volltext: http://dx.doi.org/10.1016/j.ejmg.2014.03.010
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Author Notes:Chana Vinkler, Esther Leshinsky-Silver, Marina Michelson, Dorothea Haas, Tally Lerman-Sagie, Dorit Lev
Description
Item Description:Gesehen am 24.11.2015
Physical Description:Online Resource
ISSN:1878-0849
DOI:10.1016/j.ejmg.2014.03.010