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Munis Dundar

Showing results (11-20 of 109) with videos related to

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Clinical Genetics|June 16, 2025
First Report of a Novel Pathogenic Variant in the RREB1 Gene Associated With Obesity and Metabolic SyndromeNurana Mammadova, A Baki Yildirim, Nihal Hatipoglu, et al.
Global Medical Genetics|May 14, 2021
The Story of a Ship Journey, Malaria, and the <i>HBB</i> Gene IVS-II-745 Mutation: Circassian Immigration to CyprusMahmut C Ergoren, Sehime G Temel, Gamze Mocan, et al.
The Indian Journal of Medical Research|January 31, 2009
Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)Munis Dundar, Ahmet Okay Caglayan Cetin Saatci, Korhan Arslan, et al.
Annales De Genetique|April 2, 2003
A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotypeYusuf Ozkul, M Emre Atabek, Munis Dundar, et al.
Journal of Preventive Medicine and Hygiene|December 8, 2022
Periconceptional Mediterranean diet during pregnancy on children's healthHavva Çobanoğullari, Mahmut Cerkez Ergoren, Munis Dundar, et al.
Molecular Biology Reports|December 15, 2010
Common Familial Mediterranean Fever gene mutations in a Turkish cohortMunis Dundar, Elif Funda Emirogullari, Aslihan Kiraz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 15, 2008
ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome featuresThomas Eggermann, Esther Meyer, A Okay Caglayan, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|July 19, 2016
Genetic expressions of thrombophilic factors in patients with Sheehan's syndromeFahri Bayram, Halit Diri, Elif Funda Sener, et al.
European Journal of Dentistry|February 26, 2015
Genetic background of supernumerary teethAslı Subasioglu, Selcuk Savas, Ebru Kucukyilmaz, et al.
Journal of Pediatric Hematology/Oncology|January 15, 2026
Germline Homozygous RAG1 Missense Variant Associated With Epstein-Barr Virus Negative Childhood Burkitt Lymphoma: A Case ReportNurana Mammadova, Abdulbaki Yildirim, Nuriye Gokce, et al.
Pageof 11

Showing results (11-20 of 109) with videos related to

Sort By:
Pageof 11
Clinical Genetics|June 16, 2025
First Report of a Novel Pathogenic Variant in the RREB1 Gene Associated With Obesity and Metabolic SyndromeNurana Mammadova, A Baki Yildirim, Nihal Hatipoglu, et al.
Global Medical Genetics|May 14, 2021
The Story of a Ship Journey, Malaria, and the <i>HBB</i> Gene IVS-II-745 Mutation: Circassian Immigration to CyprusMahmut C Ergoren, Sehime G Temel, Gamze Mocan, et al.
The Indian Journal of Medical Research|January 31, 2009
Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)Munis Dundar, Ahmet Okay Caglayan Cetin Saatci, Korhan Arslan, et al.
Annales De Genetique|April 2, 2003
A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotypeYusuf Ozkul, M Emre Atabek, Munis Dundar, et al.
Journal of Preventive Medicine and Hygiene|December 8, 2022
Periconceptional Mediterranean diet during pregnancy on children's healthHavva Çobanoğullari, Mahmut Cerkez Ergoren, Munis Dundar, et al.
Molecular Biology Reports|December 15, 2010
Common Familial Mediterranean Fever gene mutations in a Turkish cohortMunis Dundar, Elif Funda Emirogullari, Aslihan Kiraz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 15, 2008
ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome featuresThomas Eggermann, Esther Meyer, A Okay Caglayan, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|July 19, 2016
Genetic expressions of thrombophilic factors in patients with Sheehan's syndromeFahri Bayram, Halit Diri, Elif Funda Sener, et al.
European Journal of Dentistry|February 26, 2015
Genetic background of supernumerary teethAslı Subasioglu, Selcuk Savas, Ebru Kucukyilmaz, et al.
Journal of Pediatric Hematology/Oncology|January 15, 2026
Germline Homozygous RAG1 Missense Variant Associated With Epstein-Barr Virus Negative Childhood Burkitt Lymphoma: A Case ReportNurana Mammadova, Abdulbaki Yildirim, Nuriye Gokce, et al.
Pageof 11