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  1. 3321
    Clinical Report of a 17q12 Microdeletion with Additionally Unreported Clinical Features

    Clinical Report of a 17q12 Microdeletion with Additionally Unreported Clinical Features by Jennifer L. Roberts, Stephanie K. Gandomi, Melissa Parra, Ira Lu, Chia-Ling Gau, Majed Dasouki, Merlin G. Butler

    Published 2014-01-01
    “…Case Reports in Genetics…”
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  2. 3322
    Tıp fakülteleri temsilcileri tıp eğitimi çalıştayı; Bir çalıştayın ardından

    Tıp fakülteleri temsilcileri tıp eğitimi çalıştayı; Bir çalıştayın ardından by Oktay Sarı, Duygu Fındık, Ayşen Melek Aytuğ Koşan, Şerefnur Öztürk

    Published 2014-01-01
    “…Genel Tıp Dergisi…”
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  3. 3323
    Molecular Cytogenetic Characterization of a Non-Robertsonian Dicentric Chromosome 14;19 Identified in a Girl with Short Stature and Amenorrhea

    Molecular Cytogenetic Characterization of a Non-Robertsonian Dicentric Chromosome 14;19 Identified in a Girl with Short Stature and Amenorrhea by Usha R. Dutta, Vijaya Kumar Pidugu, Ashwin Dalal

    Published 2012-01-01
    “…Case Reports in Genetics…”
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  4. 3324
    Çocukluk çağı disgerminom tedavi sonuçları

    Çocukluk çağı disgerminom tedavi sonuçları by Buket Kara, Hilal Akbaş, İlhan Çiftçi, Yavuz Köksal

    Published 2021-09-01
    “…Genel Tıp Dergisi…”
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  5. 3325
    Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes

    Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes by Matthew J. Garabedian, Donna Wallerstein, Nubia Medina, James Byrne, Robert J. Wallerstein

    Published 2012-01-01
    “…Case Reports in Genetics…”
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  6. 3326
    Bilimsel Haritalama Yöntemiyle Hastane Yönetimi Alanındaki Tematik Değişimin Analizi

    Bilimsel Haritalama Yöntemiyle Hastane Yönetimi Alanındaki Tematik Değişimin Analizi by Esin Özdemir, Hüseyin Demir, Levent Bekir Kıdak

    Published 2017-06-01
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  7. 3327
    Psödohipoparatiroidi Tip 2: Olgu Sunumu

    Psödohipoparatiroidi Tip 2: Olgu Sunumu by Özlem Güleç Şen, Emre Kaçar, Tolga Altuğ Şen

    Published 2021-06-01
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  8. 3328
    Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case

    Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case by A. H. Sabir, G. Ryan, Z. Mohammed, J. Kirk, N. Kiely, M. Thyagarajan, T. Cole

    Published 2019-01-01
    “…Case Reports in Genetics…”
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  9. 3329
    Prenatal Diagnosis of Fetal Peters’ Plus Syndrome: A Case Report

    Prenatal Diagnosis of Fetal Peters’ Plus Syndrome: A Case Report by Neerja Gupta, Anita Kaul, Madhulika Kabra

    Published 2013-01-01
    “…Case Reports in Genetics…”
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  10. 3330
    Prescribing Drugs to Pregnant Women in Primary Healthcare

    Prescribing Drugs to Pregnant Women in Primary Healthcare by İzzet Fidancı

    Published 2024-02-01
    “…Genel Tıp Dergisi…”
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  11. 3331
    Açık kalp cerrahisinde geçici epikardiyal pacemaker tellerinin kullanılmasının klinik önemi

    Açık kalp cerrahisinde geçici epikardiyal pacemaker tellerinin kullanılmasının klinik önemi by Fatih Tomrukçu, Mustafa Büyükateş, Elif Coşkun

    Published 2015-09-01
    “…Genel Tıp Dergisi…”
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  12. 3332
    Unusual Presentation of Pelizaeus-Merzbacher Disease: Female Patient with Deletion of the Proteolipid Protein 1 Gene

    Unusual Presentation of Pelizaeus-Merzbacher Disease: Female Patient with Deletion of the Proteolipid Protein 1 Gene by Teva Brender, Donna Wallerstein, John Sum, Robert Wallerstein

    Published 2015-01-01
    “…Case Reports in Genetics…”
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  13. 3333
    A Rare Case of Severe Congenital RYR1-Associated Myopathy

    A Rare Case of Severe Congenital RYR1-Associated Myopathy by Nicola Laforgia, Manuela Capozza, Lucrezia De Cosmo, Antonio Di Mauro, Maria Elisabetta Baldassarre, Francesca Mercadante, Anna Laura Torella, Vincenzo Nigro, Nicoletta Resta

    Published 2018-01-01
    “…Case Reports in Genetics…”
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  14. 3334
    Tıp fakültesi araştırma görevlilerinde tükenmişlik sendromu ve ilişkili faktörlerin değerlendirilmesi

    Tıp fakültesi araştırma görevlilerinde tükenmişlik sendromu ve ilişkili faktörlerin değerlendirilmesi by Mustafa Armutlukuyu, Nisa Çetin Kargın, Kamile Marakoğlu

    Published 2013-01-01
    “…Genel Tıp Dergisi…”
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  15. 3335
    Sol internal torasik arterin proksimalinden çıkan gelişmiş aksesuar yan dal ve klinik önemi

    Sol internal torasik arterin proksimalinden çıkan gelişmiş aksesuar yan dal ve klinik önemi by Veli Çağlar, Şeref Alpsoy, Dursun Çayan Akkoyun, Aydın Akyüz, Ramazan Uygur

    Published 2013-01-01
    “…Genel Tıp Dergisi…”
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  16. 3336
    Mask-Related Headache Among Health Workers During COVID-19 Pandemics: Study from Somalia

    Mask-Related Headache Among Health Workers During COVID-19 Pandemics: Study from Somalia by Mehmet Ufuk Aluçlu, Nor Osman Sidow, Ahmed Muhammad Bashir, Mohamed Sheikh Hassan, Yavuz Yücel

    Published 2023-08-01
    “…Genel Tıp Dergisi…”
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  17. 3337
    A variant W chromosome in Centromochlus heckelii (Siluriformes, Auchenipteridae) and the role of repeated DNA in its heteromorphism

    A variant W chromosome in Centromochlus heckelii (Siluriformes, Auchenipteridae) and the role of repeated DNA in its heteromorphism by Chrystian Aparecido Grillo Haerter, Patrik Ferreira Viana, Fábio Hiroshi Takagui, Sandro Tonello, Vladimir Pavan Margarido, Daniel Rodrigues Blanco, Josiane Baccarin Traldi, Roberto Laridondo Lui, Eliana Feldberg

    Published 2025-01-01
    “…Genetics and Molecular Biology…”
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  18. 3338
    Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome

    Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome by Tanjung A. Sumekar, Aneel A. Ashrani, Tri I. Winarni, Randi J. Hagerman

    Published 2011-01-01
    “…Case Reports in Genetics…”
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  19. 3339
    Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations

    Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations by Nirmala D. Sirisena, U. Kalpani S. Wijetunge, Ramya de Silva, Vajira H. W. Dissanayake

    Published 2013-01-01
    “…Case Reports in Genetics…”
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  20. 3340
    Laparoskopik kolesistektomide karbondioksit pnömoperitoneumun beyin natriüretik peptid ve troponin I üzerine etkileri

    Laparoskopik kolesistektomide karbondioksit pnömoperitoneumun beyin natriüretik peptid ve troponin I üzerine etkileri by Sevil Kurban, Hande Köksal

    Published 2015-09-01
    “…Genel Tıp Dergisi…”
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