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Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis

Clinical genetics, 2016-10, Vol.90 (4), p.334-342

2016

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Occupational health of Turkish Aegean small-scale fishermen

Occupational medicine (Oxford), 2012-03, Vol.62 (2), p.148-151

2012

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An eight‐case 1q21 region series: novel aberrations and clinical variability with new features

Journal of intellectual disability research, 2019-06, Vol.63 (6), p.548-557

2019

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Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

Nature genetics, 2000-08, Vol.25 (4), p.423-426

2000

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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

Nature genetics, 2000-08, Vol.25 (4), p.397-401

2000

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OCULOECTODERMAL SYNDROME: A NEW CASE WITH GIANT CELL GRANULOMAS AND NON-OSSIFYING FIBROMAS

Genetic counseling, 2016, Vol.27 (1), p.77

2016

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The Ecology of The Ostracoda (Crustacea) Species Obtained From Erdek Bay (The Marmara Sea, Turkey)

International Journal of Environmental Research, 2015-10, Vol.9 (4), p.1245-1258

2015

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PCB pollution and macromolecular damage in Cyprinus carpio in Buyuk Menderes River: From ecotoxicology to risk assessment

Toxicology letters, 2011-08, Vol.205, p.S121-S121

2011

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PP153—Evaluation of the Relationships Between ABCB1 C3435T and G2677T/A Polymorphisms and Clinical Response to Venlafaxine in Patients with Major Depressive Disorder

Clinical therapeutics, 2013-08, Vol.35 (8), p.e66-e66

2013

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PP146—ABCB1 C3435T Polymorphism is Associated with Susceptibility to Major Depression but not Clinical Response to Citalopram in Turkish Population

Clinical therapeutics, 2013-08, Vol.35 (8), p.e63-e64

2013

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Length-weight and length-length relationships of the bluefin tuna, Thunnus thynnus L., in the Turkish part of the eastern Mediterranean Sea

Journal of applied ichthyology, 2009-12, Vol.25 (6), p.782-784

2009

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Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population

Journal of pediatric hematology/oncology, 2017-08, Vol.39 (6), p.458-462

2017

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A patient with 9q subtelomeric deletion syndrome with additional findings

Genetic counseling, 2012-01, Vol.23 (4), p.465

2012

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Linkage analysis and a novel COL4A5 mutation in a large Turkish family with Alport syndrome

Genetic counseling, 2011-01, Vol.22 (2), p.143

2011

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A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION

Genetic counseling, 2015-01, Vol.26 (4), p.401

2015

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The impact of perioperative care on complications and short term outcome in ARM type rectovestibular fistula: An ARM-Net consortium study

Journal of pediatric surgery, 2019-08, Vol.54 (8), p.1595-1600

2019

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The very rare and little-known fishes along the coasts of Izmir (Aegean Sea, Turkey) in the past 40years (1969-2008)

Journal of applied ichthyology, 2011-12, Vol.27 (6), p.1337-1345

2011

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A case with spondylo-metaphyseal dysplasia type A4

Genetic counseling, 2004, Vol.15 (3), p.363

2004

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Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?

Journal of medical genetics, 1998-10, Vol.35 (10), p.868-874

1998

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Monitoring of industrial and agricultural pollution by antioxidant enzyme activities and protein oxidation in carp along the River Buyuk Menderes: Preliminary implications

Toxicology letters, 2010-07, Vol.196, p.S130-S130

2010

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A case with Pyle type metaphyseal dysplasia: clinical, radiological and histological evaluation

Genetic counseling, 2003, Vol.14 (4), p.387

2003

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SRY gene amplifications and genotypings revealed the occurrence of the hidden maternal decidual cells in 46,XX karyotyped spontaneous abortions

Genetic counseling, 2010, Vol.21 (1), p.9

2010

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Gingival fibromatosis, short stature, border-line IQ, facial dysmorphism and hepatomegaly

Genetic counseling, 2005, Vol.16 (2), p.161

2005

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Dopamine D4 receptor gene and attention deficit hyperactivity disorder: A follow-up study

Neuropsychiatrie de l'enfance et de l'adolescence, 2012-07, Vol.60 (5), p.S264-S264

2012

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Determination of metric and meristics of gilt-head sea bream (Sparus aurata L., 1758) in Homa Lagoon (Izmir Bay) by using diagnostic radiographic method

Su ürünleri dergisi, 2005-01, Vol.22 (3-4), p.443-445

Percin, F

2005

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Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis

Occupational health of Turkish Aegean small-scale fishermen

An eight‐case 1q21 region series: novel aberrations and clinical variability with new features

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

OCULOECTODERMAL SYNDROME: A NEW CASE WITH GIANT CELL GRANULOMAS AND NON-OSSIFYING FIBROMAS

The Ecology of The Ostracoda (Crustacea) Species Obtained From Erdek Bay (The Marmara Sea, Turkey)

PCB pollution and macromolecular damage in Cyprinus carpio in Buyuk Menderes River: From ecotoxicology to risk assessment

PP153—Evaluation of the Relationships Between ABCB1 C3435T and G2677T/A Polymorphisms and Clinical Response to Venlafaxine in Patients with Major Depressive Disorder

PP146—ABCB1 C3435T Polymorphism is Associated with Susceptibility to Major Depression but not Clinical Response to Citalopram in Turkish Population

Length-weight and length-length relationships of the bluefin tuna, Thunnus thynnus L., in the Turkish part of the eastern Mediterranean Sea

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population

A patient with 9q subtelomeric deletion syndrome with additional findings

Linkage analysis and a novel COL4A5 mutation in a large Turkish family with Alport syndrome

A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION

The impact of perioperative care on complications and short term outcome in ARM type rectovestibular fistula: An ARM-Net consortium study

The very rare and little-known fishes along the coasts of Izmir (Aegean Sea, Turkey) in the past 40years (1969-2008)

A case with spondylo-metaphyseal dysplasia type A4

Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I?

Monitoring of industrial and agricultural pollution by antioxidant enzyme activities and protein oxidation in carp along the River Buyuk Menderes: Preliminary implications

A case with Pyle type metaphyseal dysplasia: clinical, radiological and histological evaluation

SRY gene amplifications and genotypings revealed the occurrence of the hidden maternal decidual cells in 46,XX karyotyped spontaneous abortions

Gingival fibromatosis, short stature, border-line IQ, facial dysmorphism and hepatomegaly

Dopamine D4 receptor gene and attention deficit hyperactivity disorder: A follow-up study

Determination of metric and meristics of gilt-head sea bream (Sparus aurata L., 1758) in Homa Lagoon (Izmir Bay) by using diagnostic radiographic method

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