Search research articles
Contact Us
Filters
Showing results (21-30 of 32) with videos related to
Page
of 4
Sort By:
Drug and Chemical Toxicology
|
February 25, 2012
Phototherapy causes a transient DNA damage in jaundiced newborns
Hasan Kahveci, Hasan Dogan, Ali Karaman, et al.
Pediatric Cardiology
|
April 3, 2024
Revisiting Atrioventricular Septal Defects: Exploring Chromosomal Abnormalities, Cardiac and Extracardiac Anomalies in a Contemporary Prenatal Cohort
Işıl Ayhan, Oya Demirci, Ali Şahap Odacılar, et al.
World Journal of Gastroenterology
|
April 30, 2008
Alteration of sister chromatid exchange frequencies in gastric cancer and chronic atrophic gastritis patients with and without H. pylori infection
Ali Karaman, Doğan Nasir Binici, Mehmet Eşref Kabalar, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
September 28, 2021
Foetal thoracic hypoplasia: concomitant anomalies and neonatal outcomes
Munip Akalin, Oya Demirci, Guher Bolat, et al.
Ophthalmic Genetics
|
March 29, 2016
Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort
Hatip Aydin, Murat Gunay, Gokhan Celik, et al.
Molecular and Clinical Oncology
|
February 2, 2018
Primary skeletal muscle lymphoma: A case report
Dogan Nasi R Binici, Ali Karaman, Ozge Timur, et al.
Journal of Perinatal Medicine
|
August 2, 2023
An analysis of factors affecting survival in prenatally diagnosed omphalocele
Işıl Ayhan, Oya Demirci, Lütfiye Uygur, et al.
Turkish Journal of Medical Sciences
|
August 12, 2016
Evaluation of maternal serum folate, vitamin B12, and homocysteine levels andfactor V Leiden, factor II g.20210G>A, and MTHFR variations in prenatallydiagnosed neural tube defects
Hatip Aydin, Resul Arisoy, Ali Karaman, et al.
European Journal of Medical Genetics
|
September 18, 2016
A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus
Mehmet Burak Mutlu, Arda Cetinkaya, Nermin Koc, et al.
American Journal of Medical Genetics. Part A
|
April 8, 2015
Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI
Yavuz Bayram, Hatip Aydin, Tomasz Gambin, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Drug and Chemical Toxicology
|
February 25, 2012
Phototherapy causes a transient DNA damage in jaundiced newborns
Hasan Kahveci, Hasan Dogan, Ali Karaman, et al.
Pediatric Cardiology
|
April 3, 2024
Revisiting Atrioventricular Septal Defects: Exploring Chromosomal Abnormalities, Cardiac and Extracardiac Anomalies in a Contemporary Prenatal Cohort
Işıl Ayhan, Oya Demirci, Ali Şahap Odacılar, et al.
World Journal of Gastroenterology
|
April 30, 2008
Alteration of sister chromatid exchange frequencies in gastric cancer and chronic atrophic gastritis patients with and without H. pylori infection
Ali Karaman, Doğan Nasir Binici, Mehmet Eşref Kabalar, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
September 28, 2021
Foetal thoracic hypoplasia: concomitant anomalies and neonatal outcomes
Munip Akalin, Oya Demirci, Guher Bolat, et al.
Ophthalmic Genetics
|
March 29, 2016
Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort
Hatip Aydin, Murat Gunay, Gokhan Celik, et al.
Molecular and Clinical Oncology
|
February 2, 2018
Primary skeletal muscle lymphoma: A case report
Dogan Nasi R Binici, Ali Karaman, Ozge Timur, et al.
Journal of Perinatal Medicine
|
August 2, 2023
An analysis of factors affecting survival in prenatally diagnosed omphalocele
Işıl Ayhan, Oya Demirci, Lütfiye Uygur, et al.
Turkish Journal of Medical Sciences
|
August 12, 2016
Evaluation of maternal serum folate, vitamin B12, and homocysteine levels andfactor V Leiden, factor II g.20210G>A, and MTHFR variations in prenatallydiagnosed neural tube defects
Hatip Aydin, Resul Arisoy, Ali Karaman, et al.
European Journal of Medical Genetics
|
September 18, 2016
A novel missense mutation, p.(R102W) in WNT7A causes Al-Awadi Raas-Rothschild syndrome in a fetus
Mehmet Burak Mutlu, Arda Cetinkaya, Nermin Koc, et al.
American Journal of Medical Genetics. Part A
|
April 8, 2015
Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI
Yavuz Bayram, Hatip Aydin, Tomasz Gambin, et al.
Page
of 4