Nazlı Büşra Açıkgöz

3PUBLICATIONS

17CO-AUTHORS

Developmental genetics (incl. sex determination)Adolescent healthGene and molecular therapy

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Publications (3)

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|Sep 23, 2026

Recognizing Stuve-Wiedemann syndrome in childhood: clinical insights from 11 patients with founder and novel LIFR variants.

|May 02, 2026

Fibrodysplasia ossificans progressiva in children: diagnostic pitfalls and ACVR1 genotype-phenotype spectrum.

|Jan 09, 2026

Homozygous MGME1 Variant in Turkish Siblings: First Reported Case With Successful Heart Transplantation, Expanding the Clinical Spectrum of MGME1 -Related Mitochondrial Disease.

Nazli Busra Acikgoz, Gizem Urel Demir, Yilmaz Yildiz

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Frequent Collaborators

3 joint publications

Gizem Urel Demir

3 joint publications

Gulen Eda Utine

3 joint publications

Pelin Ozlem Simsek Kiper

1 joint publications

Yilmaz Yildiz

1 joint publications

Mehmet Bugrahan Duz

1 joint publications

Nagihan Sener

1 joint publications

Safak Alpat

1 joint publications

Selman Kesici

1 joint publications

Ilker Ertugrul

1 joint publications

Dilek Yalnizoglu

Frequent Collaborators

3 joint publications

Gizem Urel Demir

3 joint publications

Gulen Eda Utine

3 joint publications

Pelin Ozlem Simsek Kiper

1 joint publications

Yilmaz Yildiz