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H Collmann

Showing results (41-50 of 45) with videos related to

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Mund-, Kiefer- Und Gesichtschirurgie : MKG|July 11, 1998
[Long-term outcome after corrective surgery of the neuro- and viscerocranium of patients with simple and syndrome-related premature craniosynostosis]E Reinhart, J Reuther, H Collmann, et al.
Mund-, Kiefer- Und Gesichtschirurgie : MKG|March 26, 2013
[Long-term results after corrective operations on the neuro- and viscero-cranium of patients with isolated and syndrome-related premature craniosynostosis]E Reinhart, J Reuther, H Collmann, et al.
Neurosurgery|November 1, 1983
Congenital hydrocephalus revealed in the inbred rat, LEW/JmsS Sasaki, H Goto, H Nagano, et al.
Orphanet Journal of Rare Diseases|June 29, 2006
Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasiaH J Girschick, P Schneider, I Haubitz, et al.
Clinical Genetics|October 19, 2007
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndromeI Wieland, C Weidner, R Ciccone, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Mund-, Kiefer- Und Gesichtschirurgie : MKG|July 11, 1998
[Long-term outcome after corrective surgery of the neuro- and viscerocranium of patients with simple and syndrome-related premature craniosynostosis]E Reinhart, J Reuther, H Collmann, et al.
Mund-, Kiefer- Und Gesichtschirurgie : MKG|March 26, 2013
[Long-term results after corrective operations on the neuro- and viscero-cranium of patients with isolated and syndrome-related premature craniosynostosis]E Reinhart, J Reuther, H Collmann, et al.
Neurosurgery|November 1, 1983
Congenital hydrocephalus revealed in the inbred rat, LEW/JmsS Sasaki, H Goto, H Nagano, et al.
Orphanet Journal of Rare Diseases|June 29, 2006
Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasiaH J Girschick, P Schneider, I Haubitz, et al.
Clinical Genetics|October 19, 2007
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndromeI Wieland, C Weidner, R Ciccone, et al.
Pageof 5