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Banu Nur

Showing results (1-10 of 23) with videos related to

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American Journal of Medical Genetics. Part A|July 30, 2019
Coronal craniosynostosis due to TCF12 mutations in patients from TurkeyElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Indian Journal of Dermatology, Venereology and Leprology|May 18, 2018
Mongolian spots combined with halo-like disappearance surrounding café au lait spotsAslı Bilgiç Temel, Cumhur Ibrahim Bassorgun, Banu Nur, et al.
Pediatric Neurology|August 19, 2019
Recent Advances in CraniosynostosisElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Turkish Journal of Medical Sciences|June 20, 2018
Early postoperative follow-up after craniosynostosis surgeryEbru Atike Ongun, Oguz Dursun, Mehmet Saim Kazan, et al.
Turkish Journal of Medical Sciences|March 19, 2025
Association of certain biochemical parameters related to bone cycle with genotype in MPS IIIB patientsSeda Gökkurt, İrem Peker Eyüboğlu, Banu Nur Güzel, et al.
Gene|March 23, 2019
TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosisGamze Koçak, Banu Nur Güzel, Ercan Mıhçı, et al.
The Turkish Journal of Pediatrics|March 3, 2023
Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variantNuray Öztürk, Gökcen Karamık, Hatice Mutlu, et al.
Gene|February 27, 2022
Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMAYunus Arikan, Sibel Berker Karauzum, Hilmi Uysal, et al.
Cytogenetic and Genome Research|July 6, 2021
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual DisabilityTuğba Karaman Mercan, Ozden Altiok Clark, Ozgur Erkal, et al.
Indian Journal of Pediatrics|March 3, 2022
Novel Gene Variants Associated with Primary Ciliary DyskinesiaDurkadin Demir Eksi, Elanur Yilmaz, A Erdem Basaran, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|July 30, 2019
Coronal craniosynostosis due to TCF12 mutations in patients from TurkeyElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Indian Journal of Dermatology, Venereology and Leprology|May 18, 2018
Mongolian spots combined with halo-like disappearance surrounding café au lait spotsAslı Bilgiç Temel, Cumhur Ibrahim Bassorgun, Banu Nur, et al.
Pediatric Neurology|August 19, 2019
Recent Advances in CraniosynostosisElanur Yilmaz, Ercan Mihci, Banu Nur, et al.
Turkish Journal of Medical Sciences|June 20, 2018
Early postoperative follow-up after craniosynostosis surgeryEbru Atike Ongun, Oguz Dursun, Mehmet Saim Kazan, et al.
Turkish Journal of Medical Sciences|March 19, 2025
Association of certain biochemical parameters related to bone cycle with genotype in MPS IIIB patientsSeda Gökkurt, İrem Peker Eyüboğlu, Banu Nur Güzel, et al.
Gene|March 23, 2019
TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosisGamze Koçak, Banu Nur Güzel, Ercan Mıhçı, et al.
The Turkish Journal of Pediatrics|March 3, 2023
Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variantNuray Öztürk, Gökcen Karamık, Hatice Mutlu, et al.
Gene|February 27, 2022
Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMAYunus Arikan, Sibel Berker Karauzum, Hilmi Uysal, et al.
Cytogenetic and Genome Research|July 6, 2021
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual DisabilityTuğba Karaman Mercan, Ozden Altiok Clark, Ozgur Erkal, et al.
Indian Journal of Pediatrics|March 3, 2022
Novel Gene Variants Associated with Primary Ciliary DyskinesiaDurkadin Demir Eksi, Elanur Yilmaz, A Erdem Basaran, et al.
Pageof 3