UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
about
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and reviewFunctional characterization of the 5' flanking region of human ubiquitin fusion degradation 1 like gene (UFD1L).The XIIth World Congress of Psychiatric Genetics. October 9-13, 2004, Dublin, Ireland.
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UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
description
im Juli 1999 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 July 1999
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в липні 1999
@uk
name
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@en
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@nl
type
label
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@en
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@nl
prefLabel
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@en
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@nl
P50
P1433
P1476
UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?
@en
P304
P356
10.1016/S0168-9525(99)01772-2
P577
1999-07-01T00:00:00Z