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![Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
- All authors
- Gregor, A.; Albrecht, B.; Bader, I.; Bijlsma, E.K.; Ekici, A.B.; Engels, H.; Hackmann, K.; Horn, D.; Hoyer, J.; Klapecki, J.; Kohlhase, J.; Maystadt, I.; Nagl, S.; Prott, E.; Tinschert, S.; Ullmann, R.; Wohlleber, E.; Woods, G.; Reis, A.; Rauch, A.; Zweier, C.
- Date
- 2011-08-09
- Journal
- BMC Medical Genetics
- Volume
- 12
- Pages
- -