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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Published in:
Nature Genetics, 2004, v. 36, n. 9, p. 955, doi. 10.1038/ng1407
By:
- Vissers, Lisenka E. L. M.;
- van Ravenswaaij, Conny M. A.;
- Admiraal, Ronald;
- Hurst, Jane A.;
- de Vries, Bert B. A.;
- Janssen, Irene M.;
- van der Vliet, Walter A.;
- Huys, Erik H. L. P. G.;
- de Jong, Pieter J.;
- Hamel, Ben C. J.;
- Schoenmakers, Eric F. P. M.;
- Brunner, Han G.;
- Veltman, Joris A.;
- van Kessel, Ad Geurts
Publication type:
Article
OMIP ‐ 081: A new 21‐monoclonal antibody 10‐color panel for diagnostic polychromatic immunophenotyping.
Published in:
Cytometry. Part A, 2022, v. 101, n. 2, p. 117, doi. 10.1002/cyto.a.24511
By:
- Huys, Erik H. L. P. G.;
- Hobo, Willemijn;
- Preijers, Frank W. M. B.
Publication type:
Article