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Mustafa Tekin

Showing results (151-160 of 235) with videos related to

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Research Square|July 1, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear MalformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Molecular Cytogenetics|September 24, 2013
Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarrayYao-Shan Fan, Xiaomei Ouyang, Jinghong Peng, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 21, 2008
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndromeAyça T Ergür, Gönül Ocal, Merih Berberoglu, et al.
Turkish Journal of Biology = Turk Biyoloji Dergisi|August 2, 2023
<i>VARS1</i> mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domainSemra Hiz, Seval Kiliç, Güney Bademci, et al.
Human Genetics|January 9, 2025
Human organoids for rapid validation of gene variants linked to cochlear malformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Nephron|May 1, 2015
HPSE2 mutations in urofacial syndrome, non-neurogenic neurogenic bladder and lower urinary tract dysfunctionBurcu Bulum, Z Birsin Özçakar, Duygu Duman, et al.
Genes|August 3, 2019
Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian PopulationErick Figueroa-Ildefonso, Guney Bademci, Farid Rajabli, et al.
American Journal of Medical Genetics. Part A|October 14, 2024
Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease NetworkNicholas A Borja, Rory J Tinker, Stephanie A Bivona, et al.
Genetic Testing and Molecular Biomarkers|July 21, 2010
Recurrent and private MYO15A mutations are associated with deafness in the Turkish populationF Basak Cengiz, Duygu Duman, Asli Sirmaci, et al.
Pageof 24

Showing results (151-160 of 235) with videos related to

Sort By:
Pageof 24
Research Square|July 1, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear MalformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Molecular Cytogenetics|September 24, 2013
Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarrayYao-Shan Fan, Xiaomei Ouyang, Jinghong Peng, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 21, 2008
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndromeAyça T Ergür, Gönül Ocal, Merih Berberoglu, et al.
Turkish Journal of Biology = Turk Biyoloji Dergisi|August 2, 2023
<i>VARS1</i> mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domainSemra Hiz, Seval Kiliç, Güney Bademci, et al.
Human Genetics|January 9, 2025
Human organoids for rapid validation of gene variants linked to cochlear malformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Nephron|May 1, 2015
HPSE2 mutations in urofacial syndrome, non-neurogenic neurogenic bladder and lower urinary tract dysfunctionBurcu Bulum, Z Birsin Özçakar, Duygu Duman, et al.
Genes|August 3, 2019
Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian PopulationErick Figueroa-Ildefonso, Guney Bademci, Farid Rajabli, et al.
American Journal of Medical Genetics. Part A|October 14, 2024
Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease NetworkNicholas A Borja, Rory J Tinker, Stephanie A Bivona, et al.
Genetic Testing and Molecular Biomarkers|July 21, 2010
Recurrent and private MYO15A mutations are associated with deafness in the Turkish populationF Basak Cengiz, Duygu Duman, Asli Sirmaci, et al.
Pageof 24