D. Erçal

发表

Nadir Görülen Bir Turner Sendromu Karyotipi: 45,X/47,XXX A Rare Karyotype of Turner Syndrome: 45.X/47.XXX

Olgu Sunumu, K. Demir, A. Abacı, 2014 .

Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum

E. Özer, D. Erçal, Seda Çakmaklı, 2018, Cytogenetic and Genome Research.

Clinical and Cytogenetic Evaluations of Patients with Turner Syndrome: Are We Aware Enough?

E. Bora, D. Erçal, N. Ünal, 2017 .

Congenital cardiac defects with 22q11 deletion.

T. Meşe, E. Bora, D. Erçal, 2003, The Turkish journal of pediatrics.

Genetic Evaluation of Common Neurocutaneous Syndromes.

D. Erçal, S. Gürsoy, D. Ercal, 2018, Pediatric neurology.

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

A. Caglayan, O. Ozdemır, S. Artan, 2022, Functional & Integrative Genomics.

Prevalence of Prader-Willi syndrome among infants with hypotonia.

B. Tuysuz, D. Erçal, N. Erginel-Unaltuna, 2014, The Journal of pediatrics.