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Hamide Betul Gerik-Celebi
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Journal Articles

Concomitant Mosaic Turner Syndrome and Congenital Adrenal Hyperplasia in 1 of 3 Patients of USP9X Variant-Associated Autism Spectrum Disorder

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Subject Area:
Genetics
Ahmet Güleç, Hamide Betul Gerik-Celebi, Meliha Demiral
Journal: Molecular Syndromology
Mol Syndromol (2025)
https://doi.org/10.1159/000543957
Published Online: 03 February 2025
View article titled, Concomitant Mosaic Turner Syndrome and Congenital Adrenal Hyperplasia in 1 of 3 Patients of USP9X Variant-Associated Autism Spectrum Disorder
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Journal Articles

Investigation of Genetic Changes in Three Families with Bipolar Disease

Free
Subject Area:
Genetics
Esra Çolak-Geniş, Müjdan Özdemir Erdoğan, Fethi Sırrı Çam, Ömer Aydemir, Funda Akin, Hamide Betül Gerik-Celebi, Mustafa Solak
Journal: Molecular Syndromology
Mol Syndromol (2024) 15 (6): 464–473.
https://doi.org/10.1159/000539115
Published Online: 14 June 2024
View article titled, Investigation of Genetic Changes in Three Families with Bipolar Disease
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Journal Articles

Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders

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Subject Area:
Endocrinology , Further Areas , Genetics , Women's and Children's Health
Hamide Betul Gerik-Celebi, Gul Unsel-Bolat, Hilmi Bolat
Journal: Molecular Syndromology
Mol Syndromol (2024) 15 (1): 22–29.
https://doi.org/10.1159/000534123
Published Online: 16 October 2023
View article titled, Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders
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Journal Articles

Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy

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Subject Area:
Karger e-Journal Backfile Collection 2023 , Endocrinology , Further Areas , Genetics , Women's and Children's Health
Hamide Betul Gerik-Celebi, Hilal Aydin, Hilmi Bolat, Gul Unsel-Bolat
Journal: Molecular Syndromology
Mol Syndromol (2023) 14 (3): 208–218.
https://doi.org/10.1159/000529018
Published Online: 06 June 2023
View article titled, Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy
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