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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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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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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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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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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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Can low serum brain‐derived neurotrophic factor levels be associated with lifelong premature ejaculation?; A pilot study

Andrologia, 2020-11, Vol.52 (10), p.e13746-n/a

2020

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PP01.1 – 2565: Next generation sequencing analysis in neonatal/early epileptic encephalopathy

European journal of paediatric neurology, 2015-05, Vol.19, p.S29-S29

2015

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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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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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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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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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PP12.11 – 2550: Atypical forms of 4H leukodystrophy

European journal of paediatric neurology, 2015-05, Vol.19, p.S80-S80

2015

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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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Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation

Genetic counseling, 2013, Vol.24 (2), p.179

2013

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Unusual case of difficult double-lumen endotracheal tube removal

Journal of clinical anesthesia, 2009-11, Vol.21 (7), p.514-516

2009

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D49 LUNG INFECTION CASE REPORTS II: INFECTIONS OTHER THAN FUNGAL INFECTIONS: Bordetella Bronchiseptica Pneumonia: A Case Report

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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A Comparison of Efficacy Between Two Natural Exogenous Surfactant Preparations in Premature Infants with Respiratory Distress Syndrome

Klinische Pädiatrie, 2004-07, Vol.216 (4), p.230-235

2004

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A New Mutation in the TBX5 Gene in Holt-Oram Syndrome: Two Cases in the Same Family and Prenatal Diagnosis

Journal of tropical pediatrics (1980), 2014-06, Vol.60 (3), p.257-259

2014

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THE ROLE OF ARTHROSCOPY IN WRIST ARTHRITIS

Hand clinics, 1999-08, Vol.15 (3), p.489-494

1999

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Öğrencilerin Selçuk Üniversitesi, Alaeddin Keykubad Kampüsü’ne Yönelik Suç Korkusu

İnönü Üniversitesi Sanat ve Tasarım Dergisi, 2020-12, Vol.10 (22), p.1-21

2020

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Korunan Alanların Ziyaretçi Yönetiminde Normatif Yaklaşım

İnönü Üniversitesi Sanat ve Tasarım Dergisi, 2019-12, Vol.9 (20), p.18-29

BİNGÜL, M. Bihter

2019

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STEAM EĞİTİMİNDE SANATIN YERİ

İnönü Üniversitesi Sanat ve Tasarım Dergisi, 2019-06, Vol.9 (19), p.28-41

MERCİN, Levent

2019

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Universal health coverage in Indonesia: concept, progress, and challenges

The Lancet (British edition), 2019-01, Vol.393 (10166), p.75-102

2019

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Vascular microanastomosis through an endoscopic approach: Feasibility study on two cadaver forearms

Chirurgie de la main, 2013-06, Vol.32 (3), p.136-140

2013

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Kilis Kentsel Sit Alanında Kullanıcı Odaklı Mekânsal Algı Belirlemeleri

İnönü Üniversitesi Sanat ve Tasarım Dergisi, 2018-12, Vol.8 (18), p.1-16

2018

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

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

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

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

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

Can low serum brain‐derived neurotrophic factor levels be associated with lifelong premature ejaculation?; A pilot study

PP01.1 – 2565: Next generation sequencing analysis in neonatal/early epileptic encephalopathy

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

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

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

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

PP12.11 – 2550: Atypical forms of 4H leukodystrophy

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

Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation

Unusual case of difficult double-lumen endotracheal tube removal

D49 LUNG INFECTION CASE REPORTS II: INFECTIONS OTHER THAN FUNGAL INFECTIONS: Bordetella Bronchiseptica Pneumonia: A Case Report

A Comparison of Efficacy Between Two Natural Exogenous Surfactant Preparations in Premature Infants with Respiratory Distress Syndrome

A New Mutation in the TBX5 Gene in Holt-Oram Syndrome: Two Cases in the Same Family and Prenatal Diagnosis

THE ROLE OF ARTHROSCOPY IN WRIST ARTHRITIS

Öğrencilerin Selçuk Üniversitesi, Alaeddin Keykubad Kampüsü’ne Yönelik Suç Korkusu

Korunan Alanların Ziyaretçi Yönetiminde Normatif Yaklaşım

STEAM EĞİTİMİNDE SANATIN YERİ

Universal health coverage in Indonesia: concept, progress, and challenges

Vascular microanastomosis through an endoscopic approach: Feasibility study on two cadaver forearms

Kilis Kentsel Sit Alanında Kullanıcı Odaklı Mekânsal Algı Belirlemeleri

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