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F Apaydin

Showing results (1-10 of 8) with videos related to

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Revue De Laryngologie - Otologie - Rhinologie|January 1, 1992
The evaluation of the changes of voice registers in trainee singers by using the two-channel signal processing methodF Ogüt, O Cura, T Kirazli, et al.
HNO|June 1, 1996
[A computer-assisted patient databank for the ENT field]F Apaydin, O Cura, O Günhan, et al.
HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.
HNO|March 19, 2004
[Waardenburg syndrome. A heterogenic disorder with variable penetrance]F Apaydin, M Bereketoglu, O Turan, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
Genomics|November 4, 1998
A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMDM H Pfister, F Apaydin, O Turan, et al.
The Laryngoscope|May 20, 1999
Clinical evidence for dystrophin dysfunction as a cause of hearing loss in locus DFN4M H Pfister, F Apaydin, O Turan, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9S M Leal, F Apaydin, C Barnwell, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Revue De Laryngologie - Otologie - Rhinologie|January 1, 1992
The evaluation of the changes of voice registers in trainee singers by using the two-channel signal processing methodF Ogüt, O Cura, T Kirazli, et al.
HNO|June 1, 1996
[A computer-assisted patient databank for the ENT field]F Apaydin, O Cura, O Günhan, et al.
HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.
HNO|March 19, 2004
[Waardenburg syndrome. A heterogenic disorder with variable penetrance]F Apaydin, M Bereketoglu, O Turan, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
Genomics|November 4, 1998
A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMDM H Pfister, F Apaydin, O Turan, et al.
The Laryngoscope|May 20, 1999
Clinical evidence for dystrophin dysfunction as a cause of hearing loss in locus DFN4M H Pfister, F Apaydin, O Turan, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9S M Leal, F Apaydin, C Barnwell, et al.
Pageof 1