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:
CreatorsEmailORCIDORCID Put Code
Capecchi, G.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Baldassarri, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Ferranti, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Guidoni, E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Cioni, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nuernberg, P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Mencarelli, M. A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Renieri, A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Grosso, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
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:
KeywordsLanguage
Genetics & HeredityMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/18875

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