Khayyat, Arwa Ishaq A. (2020). Genomic and molecular investigations of a large Pakistani family manifesting syndromic intellectual disability associated with microcephaly. Thesis Abstract, Universität zu Köln.
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| Item Type: | Thesis Abstract |
| Translated title: | Title Language UNSPECIFIED English |
| Creators: | Creators Email ORCID ORCID Put Code Khayyat, Arwa Ishaq A. aalkhyyat@hotmail.com UNSPECIFIED UNSPECIFIED |
| URN: | urn:nbn:de:hbz:38-111295 |
| Date: | 24 April 2020 |
| Language: | English |
| Faculty: | Faculty of Medicine |
| Divisions: | Faculty of Medicine > Biochemie > Institut I für Biochemie |
| Subjects: | Medical sciences Medicine |
| Uncontrolled Keywords: | Keywords Language Primary microcephaly UNSPECIFIED C1orf131 UNSPECIFIED Nucleolus UNSPECIFIED |
| Date of oral exam: | 22 April 2020 |
| Referee: | Name Academic Title Nürnberg, Peter Prof. Dr. Cirak, Sebahattin Dr. Korotkova, Tatiana Prof. Dr. Scholz, Henrike Prof. Dr. |
| Funders: | King Saud University, Riyadh, Saudi Arabia, Center for Molecular Medicine, Cologne, Germany |
| Refereed: | Yes |
| URI: | http://kups.ub.uni-koeln.de/id/eprint/11129 |
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