Universität zu Köln

Capecchi, G., Baldassarri, M., Ferranti, S., Guidoni, E., Cioni, M., Nuernberg, P., Mencarelli, M. A., Renieri, A. and Grosso, S. (2018). CKAP2L mutation confirms the diagnosis of Filippi syndrome. Clin. Genet., 93 (5). S. 1109 - 1111. HOBOKEN: WILEY. ISSN 1399-0004

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Item Type:	Journal Article
Creators:	Creators Email ORCID ORCID Put Code Capecchi, G. UNSPECIFIED UNSPECIFIED UNSPECIFIED Baldassarri, M. UNSPECIFIED UNSPECIFIED UNSPECIFIED Ferranti, S. UNSPECIFIED UNSPECIFIED UNSPECIFIED Guidoni, E. UNSPECIFIED UNSPECIFIED UNSPECIFIED Cioni, M. UNSPECIFIED UNSPECIFIED UNSPECIFIED Nuernberg, P. UNSPECIFIED UNSPECIFIED UNSPECIFIED Mencarelli, M. A. UNSPECIFIED UNSPECIFIED UNSPECIFIED Renieri, A. UNSPECIFIED UNSPECIFIED UNSPECIFIED Grosso, S. UNSPECIFIED UNSPECIFIED UNSPECIFIED
URN:	urn:nbn:de:hbz:38-188752
DOI:	10.1111/cge.13188
Journal or Publication Title:	Clin. Genet.
Volume:	93
Number:	5
Page Range:	S. 1109 - 1111
Date:	2018
Publisher:	WILEY
Place of Publication:	HOBOKEN
ISSN:	1399-0004
Language:	English
Faculty:	Unspecified
Divisions:	Unspecified
Subjects:	no entry
Uncontrolled Keywords:	Keywords Language Genetics & Heredity Multiple languages
Refereed:	Yes
URI:	http://kups.ub.uni-koeln.de/id/eprint/18875