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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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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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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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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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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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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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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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MEGALOCORNEA SHOULD BE INVESTIGATED IN CASES WITH HYPOTONIA AND MENTAL RETARDATION: NEUHAUSER SYNDROME--AN EASILY MISSED DIAGNOSIS

Genetic counseling, 2015, Vol.26 (4), p.443

2015

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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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Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population

Genetics and molecular research, 2011-10, Vol.10 (4), p.4126-4132

2011

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Lupus anticoagulant and protein S deficiency in otherwise healthy children with acute varicella infection

Acta Paediatrica, 2000-10, Vol.89 (10), p.1186-1189

2000

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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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Testing the psychosis continuum: differential impact of genetic and nongenetic risk factors and comorbid psychopathology across the entire spectrum of psychosis

Schizophrenia bulletin, 2012-09, Vol.38 (5), p.992-1002

2012

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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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Multiple Pterygium Syndrome

Indian journal of pediatrics, 1997, Vol.64 (1), p.113-116

1997

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Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney

Genetic counseling, 2012, Vol.23 (1), p.77

2012

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A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization

Genetic counseling, 2014-01, Vol.25 (4), p.433

2014

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Long-term evaluation of chromosomal breakages after radioisotope synovectomy for treatment of target joints in patients with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-05, Vol.16 (3), p.474-478

2010

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Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experience

Genetic counseling, 2013, Vol.24 (2), p.167

2013

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Effects of Manisa propolis on telomerase activity in leukemia cells obtained from the bone marrow of leukemia patients

International journal of food sciences and nutrition, 2009-11, Vol.60 (7), p.601-605

2009

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A case of Marden‐Walker syndrome with Dandy‐Walker malformation

Clinical genetics, 1995-04, Vol.47 (4), p.221-223

1995

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

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

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

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

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

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

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

MEGALOCORNEA SHOULD BE INVESTIGATED IN CASES WITH HYPOTONIA AND MENTAL RETARDATION: NEUHAUSER SYNDROME--AN EASILY MISSED DIAGNOSIS

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

Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population

Lupus anticoagulant and protein S deficiency in otherwise healthy children with acute varicella infection

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

Testing the psychosis continuum: differential impact of genetic and nongenetic risk factors and comorbid psychopathology across the entire spectrum of psychosis

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

Multiple Pterygium Syndrome

Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney

A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization

Long-term evaluation of chromosomal breakages after radioisotope synovectomy for treatment of target joints in patients with haemophilia

Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experience

Effects of Manisa propolis on telomerase activity in leukemia cells obtained from the bone marrow of leukemia patients

A case of Marden‐Walker syndrome with Dandy‐Walker malformation

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