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Ozgül M Alper

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

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Electrophoresis|August 10, 2004
Detection of CFTR mutations using temporal temperature gradient gel electrophoresisLee-Jun C Wong, Ozgül M Alper
Fertility and Sterility|October 16, 2004
The necessity of complete CFTR mutational analysis of an infertile couple before in vitro fertilizationLee-Jun C Wong, Ozgül M Alper, Evelyn Hsu, et al.
Pediatric Neurology|March 25, 2014
Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature reviewBanu G Nur, Suray Pehlivanoğlu, Ercan Mıhçı, et al.
Human Reproduction (Oxford, England)|May 21, 2005
Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferensChien-Chih Wu, Ozgül M Alper, Jyh-Feng Lu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 23, 2003
Detection of novel CFTR mutations in Taiwanese cystic fibrosis patientsOzgül M Alper, San-Ging Shu, Mei-Hui Lee, et al.
Cancer Research|February 12, 2004
Simultaneous suppression of epidermal growth factor receptor and c-erbB-2 reverses aneuploidy and malignant phenotype of a human ovarian carcinoma cell lineSvetlana D Pack, Ozgül M Alper, Kurt Stromberg, et al.
Human Mutation|September 15, 2004
Identification of novel and rare mutations in California Hispanic and African American cystic fibrosis patientsOzgül M Alper, Lee-Jun C Wong, Suzanne Young, et al.
Human Mutation|June 5, 2007
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearingNevra Nal, Zubair M Ahmed, Engin Erkal, et al.
Pageof 1

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

Sort By:
Pageof 1
Electrophoresis|August 10, 2004
Detection of CFTR mutations using temporal temperature gradient gel electrophoresisLee-Jun C Wong, Ozgül M Alper
Fertility and Sterility|October 16, 2004
The necessity of complete CFTR mutational analysis of an infertile couple before in vitro fertilizationLee-Jun C Wong, Ozgül M Alper, Evelyn Hsu, et al.
Pediatric Neurology|March 25, 2014
Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature reviewBanu G Nur, Suray Pehlivanoğlu, Ercan Mıhçı, et al.
Human Reproduction (Oxford, England)|May 21, 2005
Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferensChien-Chih Wu, Ozgül M Alper, Jyh-Feng Lu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 23, 2003
Detection of novel CFTR mutations in Taiwanese cystic fibrosis patientsOzgül M Alper, San-Ging Shu, Mei-Hui Lee, et al.
Cancer Research|February 12, 2004
Simultaneous suppression of epidermal growth factor receptor and c-erbB-2 reverses aneuploidy and malignant phenotype of a human ovarian carcinoma cell lineSvetlana D Pack, Ozgül M Alper, Kurt Stromberg, et al.
Human Mutation|September 15, 2004
Identification of novel and rare mutations in California Hispanic and African American cystic fibrosis patientsOzgül M Alper, Lee-Jun C Wong, Suzanne Young, et al.
Human Mutation|June 5, 2007
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearingNevra Nal, Zubair M Ahmed, Engin Erkal, et al.
Pageof 1