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Hilal Ozdağ

Showing results (1-10 of 6) with videos related to

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Drug Discovery Today|December 30, 2009
Isotopic biomarker discovery and application in translational medicineHenry K Bayele, Arturo Chiti, Rodney Colina, et al.
American Journal of Human Genetics|January 20, 2007
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaMustafa Tekin, Burcu Oztürk Hişmi, Suat Fitoz, et al.
Pediatric Blood & Cancer|September 7, 2017
Treatment of plasminogen deficiency patients with fresh frozen plasmaHande Kızılocak, Nihal Ozdemir, Gürcan Dikme, et al.
BMC Genomics|April 28, 2006
Differential expression of selected histone modifier genes in human solid cancersHilal Ozdağ, Andrew E Teschendorff, Ahmed Ashour Ahmed, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2009
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutationsAsli Sirmaci, Duygu Duman, Hatice Oztürkmen-Akay, et al.
American Journal of Human Genetics|May 11, 2010
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing lossAsli Sirmaci, Seyra Erbek, Justin Price, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Drug Discovery Today|December 30, 2009
Isotopic biomarker discovery and application in translational medicineHenry K Bayele, Arturo Chiti, Rodney Colina, et al.
American Journal of Human Genetics|January 20, 2007
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaMustafa Tekin, Burcu Oztürk Hişmi, Suat Fitoz, et al.
Pediatric Blood & Cancer|September 7, 2017
Treatment of plasminogen deficiency patients with fresh frozen plasmaHande Kızılocak, Nihal Ozdemir, Gürcan Dikme, et al.
BMC Genomics|April 28, 2006
Differential expression of selected histone modifier genes in human solid cancersHilal Ozdağ, Andrew E Teschendorff, Ahmed Ashour Ahmed, et al.
International Journal of Pediatric Otorhinolaryngology|February 4, 2009
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutationsAsli Sirmaci, Duygu Duman, Hatice Oztürkmen-Akay, et al.
American Journal of Human Genetics|May 11, 2010
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing lossAsli Sirmaci, Seyra Erbek, Justin Price, et al.
Pageof 1