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

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Bibliographische Detailangaben
Hauptverfasser: Vinkler, Chana (VerfasserIn) , Haas, Dorothea (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2014
In: European journal of medical genetics
Year: 2014, Jahrgang: 57, Heft: 6, Pages: 288-292
ISSN:1878-0849
DOI:10.1016/j.ejmg.2014.03.010
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1016/j.ejmg.2014.03.010
Volltext
Verfasserangaben:Chana Vinkler, Esther Leshinsky-Silver, Marina Michelson, Dorothea Haas, Tally Lerman-Sagie, Dorit Lev

MARC

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