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Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology
|
June 7, 2016
Frequency of five thrombophilic polymorphisms in the Egyptian population
Arzu Ulu, Ezzat Elsobky, Mohamed Elsayed, et al.
The Journal of Pediatrics
|
May 26, 2015
MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation
Nisha Garg, Guney Bademci, Joseph Foster, et al.
Frontiers of Medicine
|
August 21, 2015
Glucagon-like peptide-2 exhibits protective effect on hepatic ischemia-reperfusion injury in rats
Naci Topaloğlu, Adem Küçük, Şule Yıldırım, et al.
Genetics Research
|
April 1, 2015
Whole-exome sequencing and its impact in hereditary hearing loss
Tahir Atik, Guney Bademci, Oscar Diaz-Horta, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2019
Autosomal dominant inheritance in a recently described ZMIZ1-related neurodevelopmental disorder: Case report of siblings and an affected parent
Kumarie Latchman, Madison Calder, Dayna Morel, et al.
Pacing and Clinical Electrophysiology : PACE
|
October 6, 2004
Assessment of ventricular repolarization in a large group of children with early onset deafness
Ercan Tutar, Mustafa Tekin, Tayfun Uçar, et al.
Molecular Genetics & Genomic Medicine
|
February 19, 2020
Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families
Arti Pandya, Alexander O'Brien, Michael Kovasala, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 2, 2007
SLC26A4 mutations are associated with a specific inner ear malformation
Suat Fitoz, Levent Sennaroğlu, Armağan Incesulu, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
November 7, 2022
Diagnostic yield of next generation sequencing gene panel assays for early-onset glaucoma in an ethnically diverse population
Maria Fernanda Villalba, Alana L Grajewski, Mustafa Tekin, et al.
Biochemical and Biophysical Research Communications
|
October 13, 2010
Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling
Nejat Mahdieh, Atefeh Shirkavand, Marzieh Raeisi, et al.
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Search research articles
Search
Showing results (41-50 of 235) with videos related to
Sort By:
Page
of 24
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology
|
June 7, 2016
Frequency of five thrombophilic polymorphisms in the Egyptian population
Arzu Ulu, Ezzat Elsobky, Mohamed Elsayed, et al.
The Journal of Pediatrics
|
May 26, 2015
MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation
Nisha Garg, Guney Bademci, Joseph Foster, et al.
Frontiers of Medicine
|
August 21, 2015
Glucagon-like peptide-2 exhibits protective effect on hepatic ischemia-reperfusion injury in rats
Naci Topaloğlu, Adem Küçük, Şule Yıldırım, et al.
Genetics Research
|
April 1, 2015
Whole-exome sequencing and its impact in hereditary hearing loss
Tahir Atik, Guney Bademci, Oscar Diaz-Horta, et al.
American Journal of Medical Genetics. Part A
|
December 14, 2019
Autosomal dominant inheritance in a recently described ZMIZ1-related neurodevelopmental disorder: Case report of siblings and an affected parent
Kumarie Latchman, Madison Calder, Dayna Morel, et al.
Pacing and Clinical Electrophysiology : PACE
|
October 6, 2004
Assessment of ventricular repolarization in a large group of children with early onset deafness
Ercan Tutar, Mustafa Tekin, Tayfun Uçar, et al.
Molecular Genetics & Genomic Medicine
|
February 19, 2020
Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families
Arti Pandya, Alexander O'Brien, Michael Kovasala, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 2, 2007
SLC26A4 mutations are associated with a specific inner ear malformation
Suat Fitoz, Levent Sennaroğlu, Armağan Incesulu, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
November 7, 2022
Diagnostic yield of next generation sequencing gene panel assays for early-onset glaucoma in an ethnically diverse population
Maria Fernanda Villalba, Alana L Grajewski, Mustafa Tekin, et al.
Biochemical and Biophysical Research Communications
|
October 13, 2010
Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling
Nejat Mahdieh, Atefeh Shirkavand, Marzieh Raeisi, et al.
Page
of 24