Hasan Arı

3PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Nanomedicine
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Publications (3)

|Jun 02, 2026
Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the "Jumping SHOX" phenomenon.

|Jul 18, 2025
Two New Families With TAF13 Variant Presenting With Syndromic 46,XY Disorder of Sex Development: Expanding the Clinical Phenotype.

Hasan Arı, Ayberk Türkyılmaz, Ayşe Burcu Doğan Arı

|May 06, 2025
Four New Patients of HHAT -Related Multiple Congenital Anomalies Syndrome (Nivelon-Nivelon-Mabille Syndrome) and a Comprehensive Literature Review.

Ayşe Burcu Doğan Arı, Hasan Arı, Ayberk Türkyılmaz

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Frequent Collaborators

3 joint publications

Ayşe Burcu Doğan Arı

3 joint publications

Şenay Savaş Erdeve

2 joint publications

Ayberk Türkyılmaz

2 joint publications

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