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A small terminal deletion 11q in a boy without Jacobsen syndrome: narrowing the critical region for the 11q Jacobsen syndrome phenotype

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Bibliographische Detailangaben
Hauptverfasser: Evers, Christina (VerfasserIn) , Janssen, Johannes W. G. (VerfasserIn) , Jauch, Anna (VerfasserIn) , Moog, Ute (VerfasserIn)
Dokumenttyp: Article (Journal) Editorial
Sprache:Englisch
Veröffentlicht: March 2012
In: American journal of medical genetics
Year: 2012, Jahrgang: 158A, Heft: 3, Pages: 680-684
ISSN:1552-4833
DOI:10.1002/ajmg.a.34433
Online-Zugang:Verlag, Pay-per-use, Volltext: http://dx.doi.org/10.1002/ajmg.a.34433
Verlag, Pay-per-use, Volltext: https://www.onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.a.34433
Volltext
Verfasserangaben:Christina Evers, Johannes W.G. Janssen, Anna Jauch, Michael Bonin, and Ute Moog

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