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Genetics and Molecular Research : GMR
|
November 8, 2011
Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population
H Bulut, M Pehlivan, S Alper, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 26, 2014
Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies
E Pariltay, A Durmaz, B Durmaz, et al.
Journal of Endocrinological Investigation
|
October 7, 2020
Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families
E Unal, A A Karakaya, A Beştaş, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 16, 2004
Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years
C Gunduz, O Cogulu, T Cankaya, et al.
Psychological Medicine
|
June 22, 2012
Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome
T Binbay, M Drukker, K Alptekin, et al.
Molecular Genetics and Metabolism Reports
|
March 22, 2021
Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel <i>NAGLU</i> gene mutations
F Ozkinay, D A Emecen, M Kose, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
T Demir, H Onay, D B Savage, et al.
Experimental Dermatology
|
January 22, 2008
Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?
K U Schallreuter, P Bahadoran, M Picardo, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Genetics and Molecular Research : GMR
|
November 8, 2011
Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population
H Bulut, M Pehlivan, S Alper, et al.
Genetic Counseling (Geneva, Switzerland)
|
July 26, 2014
Genome-wide copy number variation analysis in idiopathic intellectual disability/multiple congenital anomalies
E Pariltay, A Durmaz, B Durmaz, et al.
Journal of Endocrinological Investigation
|
October 7, 2020
Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families
E Unal, A A Karakaya, A Beştaş, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 16, 2004
Trends in cytogenetic prenatal diagnosis in a reference hospital in Izmir/Turkey: a comparative study for four years
C Gunduz, O Cogulu, T Cankaya, et al.
Psychological Medicine
|
June 22, 2012
Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome
T Binbay, M Drukker, K Alptekin, et al.
Molecular Genetics and Metabolism Reports
|
March 22, 2021
Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel <i>NAGLU</i> gene mutations
F Ozkinay, D A Emecen, M Kose, et al.
Diabetic Medicine : a Journal of the British Diabetic Association
|
January 13, 2016
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations
T Demir, H Onay, D B Savage, et al.
Experimental Dermatology
|
January 22, 2008
Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?
K U Schallreuter, P Bahadoran, M Picardo, et al.
Page
of 3