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Microcephalic osteodysplastic primordial dwarfism, with the fascinating history of "Mademoiselle Crachami"

Genetic counseling, 2013-01, Vol.24 (4), p.405

Bozkaya, O Giray

2013

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HYPOPHOSPHATASIA WITH THE ASSOCIATION OF INV(1)(q11,q21.3) AND CLEFT PALATE

Genetic counseling, 2016, Vol.27 (1), p.83

2016

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AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome

Journal of medical genetics, 2006-04, Vol.43 (4), p.334-339

2006

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Three Novel Mutations of CHD7 Gene in Two Turkish Patients with Charge Syndrome; A Double Point Mutation and an Insertion

Balkan journal of medical genetics, 2015-06, Vol.18 (1), p.65-70

2015

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Investigation of different genomic variants in familial Mediterranean fever cases with monoallelic MEFV mutation

Clinical and experimental rheumatology, 2023-10, Vol.41 (10), p.2017

2023

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SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism

Journal of medical genetics, 2004-09, Vol.41 (9), p.e113-e113

2004

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PO-0806 Multi-cystic White Matter Enlarged Virchow Robin Spaces In A 5-year-old Boy

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A517-A518

2014

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Multi-cystic white matter enlarged virchow robin spaces in a 5-year-old boy

Archives of disease in childhood, 2014-10, Vol.99 (10), p.A517

2014

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PO-0806Multi-cystic White Matter Enlarged Virchow Robin Spaces In A 5-year-old Boy

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A517-A518

2014

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Plasminogen activator inhibitor-1 and angiotensin converting enzyme gene polymorphisms in Turkish asthmatic children

Allergologia et immunopathologia, 2013-01, Vol.41 (1), p.11-16

2013

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1 Three novel CFTR mutations found in Turkish patients with cystic fibrosis

Journal of cystic fibrosis, 2007, Vol.6, p.S1-S1

2007

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162 Characteristics of the patients with cystic fibrosis

Journal of cystic fibrosis, 2007, Vol.6, p.S39-S39

2007

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A rare chromosomal rearrangement [inv (2)(p11.q13)] in a 37-year-old normal male and 45,X/46,X,+ mar in his daughter

Genetic counseling, 2005, Vol.16 (3), p.317

2005

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Activated protein C reduces endotoxin-induced white matter injury in the developing rat brain

Brain research, 2007-08, Vol.1164, p.14-23

2007

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Analyses of polymorphism for UGT11 exon 1 promoter in neonates with pathologic and prolonged jaundice

Biology of the neonate, 2003-01, Vol.83 (4), p.258-262

2003

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ADAM33 Gene Polymorphisms Are Not Associated with Asthma in Turkish Children

Pediatric allergy, immunology, and pulmonology, 2012-06, Vol.25 (2), p.97-100

2012

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An unusual case of monosomy 18p: minor malformations with speech delay

Turkish journal of pediatrics, 2005-04, Vol.47 (2), p.199-201

2005

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Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy

Turkish journal of pediatrics, 2004-10, Vol.46 (4), p.333-338

2004

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Maternal preeclampsia and jitteriness in preterm infants

Pediatrics international, 1999-10, Vol.41 (5), p.557-560

1999

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A new corrosion inhibitor for copper protection

Corrosion science, 2014-07, Vol.84, p.21-29

2014

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Resin infiltration technique and fluoride varnish on white spot lesions in children: Preliminary findings of a randomized clinical trial

Nigerian journal of clinical practice, 2018-12, Vol.21 (12), p.1564-1569

2018

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Antibiotics Alter the Expression of Genes Related to Behavioral Development in Honey Bees (Hymenoptera: Apidae)

Journal of insect science (Tucson, Ariz.), 2022-03, Vol.22 (2)

2022

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ÇEVRESEL ETKİ DEĞERLENDİRME SÜRECİNE KATILIMDA HUKUKİ ESASLAR VE ALMANYA UYGULAMASI

Erciyes Üniversitesi Hukuk Fakültesi Dergisi, 2023-04, Vol.18 (1), p.373-424

AKPINAR, Giray

2023

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Your Brain on Porn. Internet Pornography and the Emerging Science of Addiction

Culturales (Mexicali, Mexico), 2022, Vol.10

Giray, Louie

2022

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MRI and PSMA PET/CT of Biochemical Recurrence of Prostate Cancer

Radiographics, 2023-12, Vol.43 (12)

2023

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Microcephalic osteodysplastic primordial dwarfism, with the fascinating history of "Mademoiselle Crachami"

HYPOPHOSPHATASIA WITH THE ASSOCIATION OF INV(1)(q11,q21.3) AND CLEFT PALATE

AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome

Three Novel Mutations of CHD7 Gene in Two Turkish Patients with Charge Syndrome; A Double Point Mutation and an Insertion

Investigation of different genomic variants in familial Mediterranean fever cases with monoallelic MEFV mutation

SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism

PO-0806 Multi-cystic White Matter Enlarged Virchow Robin Spaces In A 5-year-old Boy

Multi-cystic white matter enlarged virchow robin spaces in a 5-year-old boy

PO-0806Multi-cystic White Matter Enlarged Virchow Robin Spaces In A 5-year-old Boy

Plasminogen activator inhibitor-1 and angiotensin converting enzyme gene polymorphisms in Turkish asthmatic children

1 Three novel CFTR mutations found in Turkish patients with cystic fibrosis

162 Characteristics of the patients with cystic fibrosis

A rare chromosomal rearrangement [inv (2)(p11.q13)] in a 37-year-old normal male and 45,X/46,X,+ mar in his daughter

Activated protein C reduces endotoxin-induced white matter injury in the developing rat brain

Analyses of polymorphism for UGT11 exon 1 promoter in neonates with pathologic and prolonged jaundice

ADAM33 Gene Polymorphisms Are Not Associated with Asthma in Turkish Children

An unusual case of monosomy 18p: minor malformations with speech delay

Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy

Maternal preeclampsia and jitteriness in preterm infants

A new corrosion inhibitor for copper protection

Resin infiltration technique and fluoride varnish on white spot lesions in children: Preliminary findings of a randomized clinical trial

Antibiotics Alter the Expression of Genes Related to Behavioral Development in Honey Bees (Hymenoptera: Apidae)

ÇEVRESEL ETKİ DEĞERLENDİRME SÜRECİNE KATILIMDA HUKUKİ ESASLAR VE ALMANYA UYGULAMASI

Your Brain on Porn. Internet Pornography and the Emerging Science of Addiction

MRI and PSMA PET/CT of Biochemical Recurrence of Prostate Cancer

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