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Asli Ece Solmaz

Ege University

19

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97

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A novel bi-allelic variant in the SDHB gene causes a severe mitochondrial complex II deficiency: a case report.

2022 Clinical Neurology and Neurosurgery
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Clinical Contrubution of Next-Generation Sequencing Multi- Gene Panel Testing for BRCA Negative High Risk Breast Cancer Patients

2021 Clinical Breast Cancer
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Mutation spectrum of the NF1 gene and genotype-phenotype correlations in Turkish patients: Seventeen novel pathogenic variants.

2021 Clinical Neurology and Neurosurgery
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Gorlin Sendromlu olgularda saptanan üç yeni PTCH1 varyantı

2021
- Asli Ece Solmaz
- Huseyin Onay
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20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey.

2021 Turkish Journal of Medical Sciences
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A case of gender developmental disorder with difficulty in molecular diagnosis: New variant in NR5A1 gene

2021
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Clinical and molecular aspects of PTEN mutations in 10 pediatric patients.

2020 Annals of Human Genetics
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BRCA1-BRCA2 Mutation Analysis Results in 910 individuals: Mutation Distribution and 8 Novel Mutations

2020 Cancer Genetics and Cytogenetics
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Multipl Skleroz ve Epigenetik

2020
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A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia

2019 Journal of Clinical Research in Pediatric Endocrinology
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