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F Ozkinay

Showing results (31-40 of 56) with videos related to

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Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girlO Cogulu, C Gunduz, E Karaca, et al.
Clinical Genetics|September 1, 1996
Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotypeF F Ozkinay, M Akisü, N Kültürsay, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probesF Ozkinay, H Kanit, H Onay, et al.
Dermatology (Basel, Switzerland)|February 14, 2012
Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29E Chabchoub, O Cogulu, B Durmaz, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
A new case of Martsolf syndromeE Bora, T Cankaya, A Alpman, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experienceB Durmaz, E Karaca, A Durmaz, et al.
Gene|April 27, 2013
Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann-Pick disease patients: mutation profile and description of a novel mutationA Aykut, E Karaca, H Onay, et al.
Endocrine Research|February 24, 2001
Triple A syndrome--clinical aspects and molecular geneticsA Huebner, S J Yoon, F Ozkinay, et al.
International Journal of Food Sciences and Nutrition|October 13, 2009
Effects of Manisa propolis on telomerase activity in leukemia cells obtained from the bone marrow of leukemia patientsO Cogulu, C Biray, C Gunduz, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
Unusual presentation of biliary atresia splenic malformation syndrome with autosomal dominant hypospadiasG Tumgor, O Cogulu, H Onay, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Duane anomaly, meningomyelocele, dextroposition of heart and localized vertebrocostal alterations with associated anomalies in a girlO Cogulu, C Gunduz, E Karaca, et al.
Clinical Genetics|September 1, 1996
Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotypeF F Ozkinay, M Akisü, N Kültürsay, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probesF Ozkinay, H Kanit, H Onay, et al.
Dermatology (Basel, Switzerland)|February 14, 2012
Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29E Chabchoub, O Cogulu, B Durmaz, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2007
A new case of Martsolf syndromeE Bora, T Cankaya, A Alpman, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experienceB Durmaz, E Karaca, A Durmaz, et al.
Gene|April 27, 2013
Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann-Pick disease patients: mutation profile and description of a novel mutationA Aykut, E Karaca, H Onay, et al.
Endocrine Research|February 24, 2001
Triple A syndrome--clinical aspects and molecular geneticsA Huebner, S J Yoon, F Ozkinay, et al.
International Journal of Food Sciences and Nutrition|October 13, 2009
Effects of Manisa propolis on telomerase activity in leukemia cells obtained from the bone marrow of leukemia patientsO Cogulu, C Biray, C Gunduz, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
Unusual presentation of biliary atresia splenic malformation syndrome with autosomal dominant hypospadiasG Tumgor, O Cogulu, H Onay, et al.
Pageof 6