Two siblings with GAPO syndrome: a novel missense variant in ANTXR1
Yildiz, Onur, Taşdelen, Elifcan, Karakaya, Taner, Taşdelen, Harun
Published in Clinical dysmorphology (01.10.2022)
Published in Clinical dysmorphology (01.10.2022)
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Journal Article
Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature
Taşdelen, Elifcan, Durmaz, Ceren D, Karabulut, Halil G
Published in Cytogenetic and genome research (01.01.2018)
Published in Cytogenetic and genome research (01.01.2018)
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Journal Article
Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey
Berkay, Ezgi Gizem, Elkanova, Leyla, Kalaycı, Tuğba, Uludağ Alkaya, Dilek, Altunoğlu, Umut, Cefle, Kıvanç, Mıhçı, Ercan, Nur, Banu, Taşdelen, Elifcan, Bayramoğlu, Zuhal, Karaman, Volkan, Toksoy, Güven, Güneş, Nilay, Öztürk, Şükrü, Palandüz, Şükrü, Kayserili, Hülya, Tüysüz, Beyhan, Uyguner, Zehra Oya
Published in American journal of medical genetics. Part A (01.08.2021)
Published in American journal of medical genetics. Part A (01.08.2021)
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Journal Article
Phenotypic and molecular characterization of five patients with PIK3CA‐related overgrowth spectrum (PROS)
Gökpınar İli, Ezgi, Taşdelen, Elifcan, Durmaz, Ceren Damla, Altıner, Şule, Tuncalı, Timur, Martinez‐Glez, Victor, Karabulut, Halil Gürhan, Vural, Seçil, Ceylaner, Serdar, Acar, Mustafa Oğuz, Ilgın Ruhi, Hatice
Published in American journal of medical genetics. Part A (01.06.2022)
Published in American journal of medical genetics. Part A (01.06.2022)
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Journal Article
Dual diagnosis of Ochoa syndrome and Niemann-Pick disease type B in a consanguineous family
Cesur Baltacı, Hande Nur, Taşdelen, Elifcan, Topçu, Vehap, Eminoğlu, Fatma Tuba, Karabulut, Halil Gürhan
Published in Journal of Pediatric Endocrinology & Metabolism (26.05.2021)
Published in Journal of Pediatric Endocrinology & Metabolism (26.05.2021)
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Journal Article
Novel RETREG1 (FAM134B) founder allele is linked to HSAN2B and renal disease in a Turkish family
Taşdelen, Elifcan, Calame, Daniel G., Akay, Gulsen, Mitani, Tadahiro, Fatih, Jawid M., Herman, Isabella, Du, Haowei, Coban‐Akdemir, Zeynep, Marafi, Dana, Jhangiani, Shalini N., Posey, Jennifer E., Gibbs, Richard A., Altıparmak, Taylan, Kutlay, Nüket Yürür, Lupski, James R., Pehlivan, Davut
Published in American journal of medical genetics. Part A (01.07.2022)
Published in American journal of medical genetics. Part A (01.07.2022)
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Journal Article
Genotype Phenotype Correlation of A Case Having Chromosome 3 Imbalance
Taşdelen, Elifcan, Gökpınar İli, Ezgi, Altıner, Şule, Ceylan, Ahmet Cevdet, Tuncalı, Timur
Published in Ankara Ueniversitesi Tip Fakültesi mecmuasi (17.12.2021)
Published in Ankara Ueniversitesi Tip Fakültesi mecmuasi (17.12.2021)
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Journal Article
Determination of miR-373 and miR-204 levels in neuronal exosomes in Alzheimer?s disease
TAŞDELEN, ELİFCAN, KIZIL, ERGUVAN TUĞBA ÖZEL, AYDEMİR, SABİHA TEZCAN, YALAP, ÖMER ERAY, BİNGÖL, AYŞE PETEK, KUTLAY, NÜKET
Published in Turkish journal of medical sciences (01.01.2022)
Published in Turkish journal of medical sciences (01.01.2022)
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Journal Article
Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey
Berkay, Ezgi Gizem, Elkanova, Leyla, Kalaycı, Tuğba, Uludağ Alkaya, Dilek, Altunoğlu, Umut, Cefle, Kıvanç, Mıhçı, Ercan, Nur, Banu, Taşdelen, Elifcan, Bayramoğlu, Zuhal, Karaman, Volkan, Toksoy, Güven, Güneş, Nilay, Öztürk, Şükrü, Palandüz, Şükrü, Kayserili, Hülya, Tüysüz, Beyhan, Uyguner, Zehra Oya
Published in American journal of medical genetics. Part A (01.08.2021)
Published in American journal of medical genetics. Part A (01.08.2021)
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EVALUATION OF PHENOTYPIC SPECTRUM IN A 18P DELETION SYNDROME CASE
Gokoglu, Mustafa, Tasdelen, Elifcan, Ruhi, Hatice Ilgin
Published in Erciyes Medical Journal (01.06.2017)
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Published in Erciyes Medical Journal (01.06.2017)
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