Schindler, S. and Friedrich, M. and Wagener, H. and Lorenz, B. and Preising, Markus N. (2002) Heterozygous receptor 3 in P250L mutation of fibroblast growth factor a case of isolated craniosynostosis. JOURNAL OF MEDICAL GENETICS, 39 (10). pp. 764-766. ISSN 0022-2593
Full text not available from this repository. (Request a copy)| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | CROUZON-SYNDROME; PRO250ARG MUTATION; CORONAL CRANIOSYNOSTOSIS; IDENTICAL MUTATIONS; PFEIFFER-SYNDROME; GENE CAUSE; FGFR2; |
| Subjects: | 600 Technology > 610 Medical sciences Medicine |
| Divisions: | Medicine > Abteilung für Pädiatrische Ophthalmologie, Strabismologie und Ophthalmogenetik Medicine > Lehrstuhl für Neurochirurgie |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 05 Oct 2021 05:45 |
| Last Modified: | 05 Oct 2021 05:45 |
| URI: | https://pred.uni-regensburg.de/id/eprint/39838 |
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