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R Birkenhäger

Showing results (1-10 of 22) with videos related to

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Laryngo- Rhino- Otologie|September 12, 2013
[Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening]N Prera, E Löhle, R Birkenhäger
Laryngo- Rhino- Otologie|April 5, 2007
[Non-syndromic hereditary hearing impairment]R Birkenhäger, A Aschendorff, J Schipper, et al.
Laryngo- Rhino- Otologie|January 14, 2005
[The interesting case -- case no. 67]P U Lohnstein, W Maier, R Birkenhäger, et al.
Laryngo- Rhino- Otologie|March 21, 2006
[Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?]R Birkenhäger, A J Zimmer, W Maier, et al.
European Journal of Biochemistry|September 22, 1999
F0 complex of the Escherichia coli ATP synthase. Not all monomers of the subunit c oligomer are involved in F1 interactionR Birkenhäger, J C Greie, K Altendorf, et al.
Biochimica Et Biophysica Acta|June 7, 1996
The promoter-proximal, unstable IB region of the atp mRNA of Escherichia coli: an independently degraded region that can act as a destabilizing elementH C Schramm, B Schneppe, R Birkenhäger, et al.
HNO|December 18, 2012
[Synchronous schwannoma of the vagus nerve and the cervical sympathetic chain]T F Jakob, R Birkenhäger, G Kayser, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|August 14, 2009
Rapid umbilical cord diagnostic of hereditary profound hearing loss: how we do itR Birkenhäger, W Maier, M Kunze, et al.
Laryngo- Rhino- Otologie|December 22, 2004
[Identification of two heterozygous mutations in the SLC26A4/PDS gene in a family with Pendred-syndrome]R Birkenhäger, F B Knapp, T Klenzner, et al.
European Journal of Biochemistry|May 15, 1995
The F0 complex of the Escherichia coli ATP synthase. Investigation by electron spectroscopic imaging and immunoelectron microscopyR Birkenhäger, M Hoppert, G Deckers-Hebestreit, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Laryngo- Rhino- Otologie|September 12, 2013
[Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening]N Prera, E Löhle, R Birkenhäger
Laryngo- Rhino- Otologie|April 5, 2007
[Non-syndromic hereditary hearing impairment]R Birkenhäger, A Aschendorff, J Schipper, et al.
Laryngo- Rhino- Otologie|January 14, 2005
[The interesting case -- case no. 67]P U Lohnstein, W Maier, R Birkenhäger, et al.
Laryngo- Rhino- Otologie|March 21, 2006
[Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?]R Birkenhäger, A J Zimmer, W Maier, et al.
European Journal of Biochemistry|September 22, 1999
F0 complex of the Escherichia coli ATP synthase. Not all monomers of the subunit c oligomer are involved in F1 interactionR Birkenhäger, J C Greie, K Altendorf, et al.
Biochimica Et Biophysica Acta|June 7, 1996
The promoter-proximal, unstable IB region of the atp mRNA of Escherichia coli: an independently degraded region that can act as a destabilizing elementH C Schramm, B Schneppe, R Birkenhäger, et al.
HNO|December 18, 2012
[Synchronous schwannoma of the vagus nerve and the cervical sympathetic chain]T F Jakob, R Birkenhäger, G Kayser, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|August 14, 2009
Rapid umbilical cord diagnostic of hereditary profound hearing loss: how we do itR Birkenhäger, W Maier, M Kunze, et al.
Laryngo- Rhino- Otologie|December 22, 2004
[Identification of two heterozygous mutations in the SLC26A4/PDS gene in a family with Pendred-syndrome]R Birkenhäger, F B Knapp, T Klenzner, et al.
European Journal of Biochemistry|May 15, 1995
The F0 complex of the Escherichia coli ATP synthase. Investigation by electron spectroscopic imaging and immunoelectron microscopyR Birkenhäger, M Hoppert, G Deckers-Hebestreit, et al.
Pageof 3