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Archivos Argentinos De Pediatria
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May 11, 2016
Association of Wolfram syndrome with Fallot tetralogy in a girl
Hüseyin A Korkmaz, Korcan Demir, Filiz Hazan, et al.
Case Reports in Genetics
|
July 23, 2014
Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan gene
Gulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, et al.
Pediatric Neurology
|
April 19, 2014
Sarcolemmal alpha and gamma sarcoglycan protein deficiencies in Turkish siblings with a novel missense mutation in the alpha sarcoglycan gene
Gulden Diniz, Hulya Tosun Yildirim, Gulcin Akinci, et al.
Journal of Pediatric Hematology/Oncology
|
October 20, 2015
Chronic Neutropenia in Childhood: Experience From a Single Center
Tuba H Karapinar, Yeşim Oymak, Yilmaz Ay, et al.
Indian Journal of Pediatrics
|
January 29, 2016
Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations
Tahir Atik, Ayca Aykut, Filiz Hazan, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
March 31, 2021
Identification of two <i>AMH</i> gene variants in two unrelated patients with persistent Müllerian duct syndrome: one novel variant
Sezer Acar, Özlem Nalbantoğlu, Semra Gürsoy, et al.
Archives of Endocrinology and Metabolism
|
November 10, 2023
Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes
Tarık Kırkgöz, Semra Gürsoy, Sezer Acar, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 17, 2020
Detection of <i>SHOX</i> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature
Semra Gürsoy, Filiz Hazan, Ayça Aykut, et al.
Bosnian Journal of Basic Medical Sciences
|
January 17, 2016
The association between brain natriuretic peptide and tissue Doppler parameters in children with hypertrophic cardiomyopathy
Taliha Öner, Rahmi Özdemir, Filiz Hazan, et al.
Sisli Etfal Hastanesi Tip Bulteni
|
August 22, 2022
Clinical and Genetic Characteristics of Patients with Common and Rare Types of Congenital Adrenal Hyperplasia: Novel Variants in <i>STAR</i> and <i>CYP17A1</i>
Ozge Koprulu, Behzat Ozkan, Sezer Acar, et al.
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Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Archivos Argentinos De Pediatria
|
May 11, 2016
Association of Wolfram syndrome with Fallot tetralogy in a girl
Hüseyin A Korkmaz, Korcan Demir, Filiz Hazan, et al.
Case Reports in Genetics
|
July 23, 2014
Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan gene
Gulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, et al.
Pediatric Neurology
|
April 19, 2014
Sarcolemmal alpha and gamma sarcoglycan protein deficiencies in Turkish siblings with a novel missense mutation in the alpha sarcoglycan gene
Gulden Diniz, Hulya Tosun Yildirim, Gulcin Akinci, et al.
Journal of Pediatric Hematology/Oncology
|
October 20, 2015
Chronic Neutropenia in Childhood: Experience From a Single Center
Tuba H Karapinar, Yeşim Oymak, Yilmaz Ay, et al.
Indian Journal of Pediatrics
|
January 29, 2016
Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations
Tahir Atik, Ayca Aykut, Filiz Hazan, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
March 31, 2021
Identification of two <i>AMH</i> gene variants in two unrelated patients with persistent Müllerian duct syndrome: one novel variant
Sezer Acar, Özlem Nalbantoğlu, Semra Gürsoy, et al.
Archives of Endocrinology and Metabolism
|
November 10, 2023
Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes
Tarık Kırkgöz, Semra Gürsoy, Sezer Acar, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
April 17, 2020
Detection of <i>SHOX</i> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature
Semra Gürsoy, Filiz Hazan, Ayça Aykut, et al.
Bosnian Journal of Basic Medical Sciences
|
January 17, 2016
The association between brain natriuretic peptide and tissue Doppler parameters in children with hypertrophic cardiomyopathy
Taliha Öner, Rahmi Özdemir, Filiz Hazan, et al.
Sisli Etfal Hastanesi Tip Bulteni
|
August 22, 2022
Clinical and Genetic Characteristics of Patients with Common and Rare Types of Congenital Adrenal Hyperplasia: Novel Variants in <i>STAR</i> and <i>CYP17A1</i>
Ozge Koprulu, Behzat Ozkan, Sezer Acar, et al.
Page
of 6