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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-CGH
B B Geckinli, H Aydin, A Karaman
Genetic Counseling (Geneva, Switzerland)
|
February 9, 2016
CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33
B 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 LITERATURE
By 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 Disability
A Türkyılmaz, B B Geckinli, E Tekin, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 26, 2014
Craniorachischisis, gastroschisis, and a branchial sinus defect: a case report
H Aydin, S Yanik, E Tug, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 21, 2014
Tetrasomy 12p presenting with long appendix: a prenatal case
H 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 insufficiency
B 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 Turkey
Ismail 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 Microcephaly
Nichole 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 microcephaly
Margaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Genetic Counseling (Geneva, Switzerland)
|
March 26, 2015
A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH
B B Geckinli, H Aydin, A Karaman
Genetic Counseling (Geneva, Switzerland)
|
February 9, 2016
CLINICAL REPORT OF A PATIENT WITH DE NOVO TRISOMY 12q23.1q24.33
B 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 LITERATURE
By 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 Disability
A Türkyılmaz, B B Geckinli, E Tekin, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 26, 2014
Craniorachischisis, gastroschisis, and a branchial sinus defect: a case report
H Aydin, S Yanik, E Tug, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 21, 2014
Tetrasomy 12p presenting with long appendix: a prenatal case
H 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 insufficiency
B 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 Turkey
Ismail 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 Microcephaly
Nichole 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 microcephaly
Margaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
Page
of 2