Asif, M., Kaygusuz, E., Shinawi, M., Nickelsen, A., Hochscherf, J., Lindenblatt, D., Noegel, A. A., Tinschert, S., Niefind, K., Fortugno, P., Jose, J., Brancati, F., Nuernberg, P. and Hussain, M. S. (2020). De novo pathogenic variants in CSNK2B cause a new intellectual disability-craniodigital syndrome distinguished from Poirier-Bienvenu neurodevelopmental syndrome. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 129 - 131. LONDON: SPRINGERNATURE. ISSN 1476-5438

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Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Asif, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Kaygusuz, E.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Shinawi, M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nickelsen, A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hochscherf, J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lindenblatt, D.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Noegel, A. A.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Tinschert, S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Niefind, K.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Fortugno, P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Jose, J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Brancati, F.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nuernberg, P.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Hussain, M. S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-308964
Journal or Publication Title: Eur. J. Hum. Genet.
Volume: 28
Number: SUPPL 1
Page Range: S. 129 - 131
Date: 2020
Publisher: SPRINGERNATURE
Place of Publication: LONDON
ISSN: 1476-5438
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
Biochemistry & Molecular Biology; Genetics & HeredityMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/30896

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