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B Geckinli

Showing results (1-10 of 11) with videos related to

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Genetic Counseling (Geneva, Switzerland)|March 26, 2015
A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGHB B Geckinli, H Aydin, A Karaman
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33B B Geckinli, H Aydin, A Karaman, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
CO-OCCURRENCE OF NEURAL TUBE DEFECT, THORACAL DEFECT AND OMPHALOCELE: A RARE CASE AND REVIEW OF THE LITERATUREBy H Aydin, R Arisoy, H Simsek, et al.
Balkan Journal of Medical Genetics : BJMG|October 17, 2022
Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual DisabilityA Türkyılmaz, B B Geckinli, E Tekin, et al.
Genetic Counseling (Geneva, Switzerland)|July 26, 2014
Craniorachischisis, gastroschisis, and a branchial sinus defect: a case reportH Aydin, S Yanik, E Tug, et al.
Genetic Counseling (Geneva, Switzerland)|February 21, 2014
Tetrasomy 12p presenting with long appendix: a prenatal caseH Aydin, R Arisoy, B Geckinli, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 3, 2014
Prevalence of X-aneuploidies, X-structural abnormalities and 46,XY sex reversal in Turkish women with primary amenorrhea or premature ovarian insufficiencyB B Geckinli, G Toksoy, C Sayar, et al.
Epilepsy & Behavior : E&B|March 9, 2026
Extreme ambient temperatures and seizure outcomes in children with epilepsy: insights from a survey in TurkeyIsmail Hakki Akbeyaz, Yekta Culpan, Seyhmus Gavas, et al.
Developmental Cell|November 19, 2019
Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause MicrocephalyNichole Link, Hyunglok Chung, Angad Jolly, et al.
American Journal of Human Genetics|February 1, 2023
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephalyMargaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Genetic Counseling (Geneva, Switzerland)|March 26, 2015
A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGHB B Geckinli, H Aydin, A Karaman
Genetic Counseling (Geneva, Switzerland)|February 9, 2016
CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33B B Geckinli, H Aydin, A Karaman, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
CO-OCCURRENCE OF NEURAL TUBE DEFECT, THORACAL DEFECT AND OMPHALOCELE: A RARE CASE AND REVIEW OF THE LITERATUREBy H Aydin, R Arisoy, H Simsek, et al.
Balkan Journal of Medical Genetics : BJMG|October 17, 2022
Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual DisabilityA Türkyılmaz, B B Geckinli, E Tekin, et al.
Genetic Counseling (Geneva, Switzerland)|July 26, 2014
Craniorachischisis, gastroschisis, and a branchial sinus defect: a case reportH Aydin, S Yanik, E Tug, et al.
Genetic Counseling (Geneva, Switzerland)|February 21, 2014
Tetrasomy 12p presenting with long appendix: a prenatal caseH Aydin, R Arisoy, B Geckinli, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 3, 2014
Prevalence of X-aneuploidies, X-structural abnormalities and 46,XY sex reversal in Turkish women with primary amenorrhea or premature ovarian insufficiencyB B Geckinli, G Toksoy, C Sayar, et al.
Epilepsy & Behavior : E&B|March 9, 2026
Extreme ambient temperatures and seizure outcomes in children with epilepsy: insights from a survey in TurkeyIsmail Hakki Akbeyaz, Yekta Culpan, Seyhmus Gavas, et al.
Developmental Cell|November 19, 2019
Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause MicrocephalyNichole Link, Hyunglok Chung, Angad Jolly, et al.
American Journal of Human Genetics|February 1, 2023
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephalyMargaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
Pageof 2