Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.
about
Mutation update on the CHD7 gene involved in CHARGE syndromeCHARGE syndrome: a review of the immunological aspects.Xenopus: An emerging model for studying congenital heart disease.More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated.Immunodeficiency in CHARGE syndrome.
P2860
Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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name
Combined microdeletions and CH ...... ar investigation by array-CGH.
@en
Combined microdeletions and CH ...... ar investigation by array-CGH.
@nl
type
label
Combined microdeletions and CH ...... ar investigation by array-CGH.
@en
Combined microdeletions and CH ...... ar investigation by array-CGH.
@nl
prefLabel
Combined microdeletions and CH ...... ar investigation by array-CGH.
@en
Combined microdeletions and CH ...... ar investigation by array-CGH.
@nl
P2093
P2860
P356
P1476
Combined microdeletions and CH ...... lar investigation by array-CGH
@en
P2093
Anna-Venetia Skiathitou
Aristeidis Giannakopoulos
Emmanuel Kanavakis
Helena Fryssira
Krinio Giannikou
Maria Kanariou
Marios Kaliakatsos
Tania Siahanidou
P2860
P2888
P304
P356
10.1038/JHG.2010.95
P577
2010-08-05T00:00:00Z