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Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

Scientific reports, 2016-08, Vol.6 (1), p.31622-31622, Article 31622

2016

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Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome

Psychological medicine, 2012-12, Vol.42 (12), p.2499-2510

2012

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Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations

Molecular genetics and metabolism reports, 2021-06, Vol.27, p.100732-100732, Article 100732

2021

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In vitro gene manipulation of spinal muscular atrophy fibroblast cell line using gene-targeting fragment for restoration of SMN protein expression

Gene therapy, 2016-01, Vol.23 (1), p.10-17

2016

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No relationship between lipoprotein-associated phospholipase A2, proinflammatory cytokines, and neopterin in Alzheimer's disease

Experimental gerontology, 2016-05, Vol.77, p.1-6

2016

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Successful treatment of hepatic and mesh Aspergillosis in a neonate with giant omphalocele

Journal de mycologie médicale, 2022-05, Vol.32 (2), p.101245, Article 101245

2022

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Low levels of mannose-binding lectin confers protection against tuberculosis in Turkish children

European journal of clinical microbiology & infectious diseases, 2008-12, Vol.27 (12), p.1165-1169

2008

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Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann–Pick disease patients: Mutation profile and description of a novel mutation

Gene, 2013-09, Vol.526 (2), p.484-486

2013

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Assessment of Toll-like receptor-4 gene polymorphism on pyelonephritis and renal scar

International journal of immunogenetics, 2012-08, Vol.39 (4), p.303-307

2012

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TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION

Genetic counseling, 2015-01, Vol.26 (4), p.431

2015

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558 Prader-Willi Syndrome Due to Maternal Uniparental Disomy following Assisted Reproductive Technology

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A162-A162

2012

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Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review

Journal of assisted reproduction and genetics, 2009-03, Vol.26 (2-3), p.119-122

2009

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A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS

Genetic counseling, 2016, Vol.27 (1), p.1

2016

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Results of fifteen-year follow-up from a single center: findings and risks for tumor development in isolated hemihyperplasia cases

Genetic counseling, 2014-01, Vol.25 (4), p.417

2014

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P-18 Evaluation of preimplantation genetic aneuploidy screening cases at a reference genetics center in Izmir, Turkey

Reproductive biomedicine online, 2013-05, Vol.26, p.S34-S34

2013

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P-53 Outcome of preimplantation genetic diagnosis of balanced translocation carriers

Reproductive biomedicine online, 2013-05, Vol.26, p.S47-S47

2013

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P-61 Analysis of couples having genetic counseling for preimplantation genetic diagnosis or preimplantation genetic screening

Reproductive biomedicine online, 2013-05, Vol.26, p.S50-S50

2013

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Pontocerebellar hypoplasia type III (CLAM): Extended phenotype and novel molecular findings

Journal of neurology, 2009-03, Vol.256 (3), p.416-419

2009

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THE SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH KLIPPEL-TRENAUNAY-WEBER SYNDROME

Genetic counseling, 2015-01, Vol.26 (2), p.249

2015

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EPA-1760 – Familial liability, the BDNF-VAL66MET polymorphism and psychotic-like experiences

European psychiatry, 2014, Vol.29, p.1-1

2014

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61 Association of Vitamin D Receptor Gene Polymorphisms and Bronchopulmonary Dysplasia

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A17-A18

2012

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Multigene Methylation Analysis of Conventional Renal Cell Carcinoma

Urologia internationalis, 2009-01, Vol.83 (1), p.107-112

2009

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DETERMINATION OF FETAL RHESUS D STATUS BY MATERNAL PLASMA DNA ANALYSIS

Balkan journal of medical genetics, 2013-12, Vol.16 (2), p.33-38

2013

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CONGENITAL ABSENCE OF THE PORTAL VEIN IN A CHILD WITH TURNER SYNDROME

Genetic counseling, 2015-01, Vol.26 (3), p.353

2015

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252 Whole Genome Microrna Expression Profiling in Childhood Acute Lymphoblastic Leukemia: A Prospective Evaluation

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A73-A73

2012

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Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome

Clinical and genetic features of 13 patients with mucopolysaccarhidosis type IIIB: Description of two novel NAGLU gene mutations

In vitro gene manipulation of spinal muscular atrophy fibroblast cell line using gene-targeting fragment for restoration of SMN protein expression

No relationship between lipoprotein-associated phospholipase A2, proinflammatory cytokines, and neopterin in Alzheimer's disease

Successful treatment of hepatic and mesh Aspergillosis in a neonate with giant omphalocele

Low levels of mannose-binding lectin confers protection against tuberculosis in Turkish children

Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann–Pick disease patients: Mutation profile and description of a novel mutation

Assessment of Toll-like receptor-4 gene polymorphism on pyelonephritis and renal scar

TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION

558 Prader-Willi Syndrome Due to Maternal Uniparental Disomy following Assisted Reproductive Technology

Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review

A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS

Results of fifteen-year follow-up from a single center: findings and risks for tumor development in isolated hemihyperplasia cases

P-18 Evaluation of preimplantation genetic aneuploidy screening cases at a reference genetics center in Izmir, Turkey

P-53 Outcome of preimplantation genetic diagnosis of balanced translocation carriers

P-61 Analysis of couples having genetic counseling for preimplantation genetic diagnosis or preimplantation genetic screening

Pontocerebellar hypoplasia type III (CLAM): Extended phenotype and novel molecular findings

THE SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH KLIPPEL-TRENAUNAY-WEBER SYNDROME

EPA-1760 – Familial liability, the BDNF-VAL66MET polymorphism and psychotic-like experiences

61 Association of Vitamin D Receptor Gene Polymorphisms and Bronchopulmonary Dysplasia

Multigene Methylation Analysis of Conventional Renal Cell Carcinoma

DETERMINATION OF FETAL RHESUS D STATUS BY MATERNAL PLASMA DNA ANALYSIS

CONGENITAL ABSENCE OF THE PORTAL VEIN IN A CHILD WITH TURNER SYNDROME

252 Whole Genome Microrna Expression Profiling in Childhood Acute Lymphoblastic Leukemia: A Prospective Evaluation

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