From cataract to syndrome diagnosis: Revaluation of Warburg‐Micro syndrome Type 1 patients by Mutlu Albayrak, Hatice, Elçioğlu, Nursel H., Yeter, Burcu, Karaer, Kadri

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Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia by Guo, Long, Elcioglu, Nursel H, Mizumoto, Shuji, Wang, Zheng, Noyan, Bilge, Albayrak, Hatice M, Yamada, Shuhei, Matsumoto, Naomichi, Miyake, Noriko, Nishimura, Gen, Ikegawa, Shiro

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The Spectrum of NF1 Gene Variations in Southeastern Turkey by Kirat, Emre, Albayrak, Hatice Mutlu

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Kosaki Overgrowth Syndrome: Report of a Family with a Novel PDGFRB Variant by Mutlu Albayrak, Hatice, Calder, Alistair D.

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Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience by Ergül Bozacı, Ayşe, Göksoy, Emine, Tekmenuray Ünal, Aysel, Mutlu Albayrak, Hatice, Taş, İbrahim, Kanar, Berat, Özbek, Mehmet Nuri, Köse, Melis

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Fetal Valproate Syndrome by Mutlu-Albayrak, Hatice, Bulut, Cahide, Çaksen, Hüseyin

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Comparison of radiologic findings between SARS-CoV-2 and other respiratory tract viruses in critically ill children during the COVID-19 pandemic by PERK, OKTAY, KENDİRLİ, TANIL, UYAR, EMEL, ŞEN AKOVA, BİRSEL, ALBAYRAK, HATİCE, AĞIN, HASAN, ONGUN, EBRU ATİKE, TURANLI, EŞE EDA, ŞIK, SARE GÜNTÜLÜ, SİNCAR, ŞAHİN, BOZAN, GÜRKAN, DEMİRKOL, DEMET, ÜLGEN TEKEREK, NAZAN, TALİP, MEY, OTO, ARZU, İNCEKÖY GİRGİN, FEYZA, SARI, FERHAT, KUTLU, NURETTİN ONUR, GÜNEŞ, ALTAN, FİTÖZ, ÖMER SUAT

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A congenital cranial dysinnervation disorder: Möbius' syndrome by Albayrak, Hatice Mutlu, Tarakçı, Nuriye, Altunhan, Hüseyin, Örs, Rahmi, Çaksen, Hüseyin

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Common Obesity Syndromes in Childhood by Mutlu Albayrak, Hatice, Selver Eklioglu, Beray

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Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 gene by Mutlu-Albayrak, Hatice, Karaer, Kadri

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PIGA-related epileptic encephalopathy demonstrating intrafamilial phenotypic heterogeneity by Perk Yucel, Peren, Mutlu Albayrak, Hatice

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Childhood-onset autosomal recessive ataxias: a cross-sectional study from Turkey by Mutlu-Albayrak, Hatice, Kırat, Emre, Gürbüz, Gürkan

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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations by Colombo, Elisa Adele, Mutlu-Albayrak, Hatice, Shafeghati, Yousef, Balasar, Mine, Piard, Juliette, Gentilini, Davide, Di Blasio, Anna Maria, Gervasini, Cristina, Van Maldergem, Lionel, Larizza, Lidia

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SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling by Lin, Yuh-Charn, Niceta, Marcello, Muto, Valentina, Vona, Barbara, Pagnamenta, Alistair T., Maroofian, Reza, Beetz, Christian, van Duyvenvoorde, Hermine, Dentici, Maria Lisa, Lauffer, Peter, Vallian, Sadeq, Ciolfi, Andrea, Pizzi, Simone, Bauer, Peter, Grüning, Nana-Maria, Bellacchio, Emanuele, Del Fattore, Andrea, Petrini, Stefania, Shaheen, Ranad, Tiosano, Dov, Halloun, Rana, Pode-Shakked, Ben, Albayrak, Hatice Mutlu, Işık, Emregül, Wit, Jan M., Dittrich, Marcus, Freire, Bruna L., Bertola, Debora R., Jorge, Alexander A.L., Barel, Ortal, Sabir, Ataf H., Al Tenaiji, Amal M.J., Taji, Sulaima M., Al-Sannaa, Nouriya, Al-Abdulwahed, Hind, Digilio, Maria Cristina, Irving, Melita, Anikster, Yair, Bhavani, Gandham S.L., Girisha, Katta M., Haaf, Thomas, Taylor, Jenny C., Dallapiccola, Bruno, Alkuraya, Fowzan S., Yang, Ruey-Bing, Tartaglia, Marco

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Identification of SLC22A5 Gene Mutation in a Family with Carnitine Uptake Defect by Çaksen, Hüseyin, Tanyalçın, Tijen, Oflaz, Mehmet Burhan, Bene, Judit, Mutlu-Albayrak, Hatice, Melegh, Bela

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Evaluation of 601 children with multisystem inflammatory syndrome (Turk MISC study) by Yilmaz, Dilek, Ekemen Keles, Yildiz, Emiroglu, Melike, Duramaz, Burcu Bursal, Ugur, Cuneyt, Aldemir Kocabas, Bilge, Celik, Talyan, Ozdemir, Halil, Bayturan, Semra, Turel, Ozden, Erdeniz, Emine Hafize, Cakici, Ozlem, Cakmak Taskin, Esra, Erbas, İrem Ceren, Genceli, Mustafa, Sari, Emine Ergul, Caymaz, Canan, Kizil, Mahmut Can, Sutcu, Murat, Demirbuga, Asuman, Alkan, Gulsum, Bagcı, Zafer, Timurtas Dayar, Gulperi, Ozkan, Esra Akyuz, Tekin Yilmaz, Ayse, Akca, Mehtap, Yesil, Edanur, Kara, Soner Sertan, Akturk, Hacer, Yasar, Belma, Umit, Zuhal, Uygun, Hatice, Erdem, Nurettin, Buyukcam, Ayse, Karadag Oncel, Eda, Tuter Oz, Sadiye Kubra, Cetin, Hafize Selma, Anil, Ayse Berna, Yilmaz, Resul, Zengin, Neslihan, Uzuner, Selcuk, Albayrak, Hatice, Borakay, Ozgur, Topal, Sevgi, Arslan, Gazi, Yazar, Abdullah, Ozer, Arife, Kendirli, Tanil, Kara, Emine Manolya, Demirkol, Demet, Battal, Fatih, Kosker, Muhammet, Metin Akcan, Ozge, Kihtir, Hasan Serdar, Gul, Doruk, Zararci, Kazim, Alakaya, Mehmet, Kula, Nilgun, Celik, Elif, Petmezci, Ercument, Evren, Gultac, Kara Aksay, Ahu, Konca, Capan, Sert, Ahmet, Arslan, Derya, Bornaun, Helen, Tekeli, Onur, Bal, Alkan, Sahin, Irfan Oguz, Demir, Selcan, Sap, Fatih, Akyol, Mehmet Bedir, Tanidir, Ibrahim Cansaran, Donmez, Yasemin Nuran, Ucar, Tayfun, Coban, Senay, Arga, Gul, Hancerli Torun, Selda, Karpuz, Derya, Celik, Serkan Fazli, Varan, Celal, Elmali, Ferhan, Oncel, Selim, Belet, Nursen, Hatipoglu, Nevin, Dalgic Karabulut, Nazan, Turgut, Mehmet, Somer, Ayper, Kuyucu, Necdet, Dinleyici, Ener Cagri, Ciftci, Ergin, Kara, Ates

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Influenza Virus Associated Pediatric Acute Respiratory Distress Syndrome: Clinical Characteristics and Outcomes by Yener, Nazik, Üdürgücü, Muhammed, Yılmaz, Resul, Kendirli, Tanıl, Tekerek, Nazan Ülgen, Evren, Gültaç, Arı, Hatice Feray, Yıldızdaş, Dinçer, Demirkol, Demet, Pişkin, Ethem, Duyu, Muhterem, Dalkıran, Tahir, Akçay, Nihal, Yalındağ Öztürk, Nilüfer, Yeşilbaş, Osman, Bozan, Gürkan, Gurbanov, Anar, Albayrak, Hatice

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Esophageal Atresia and Thenar Hypoplasia Associated with Asymmetric Crying Face by Mutlu-Albayrak, Hatice, Damar, Çağrı, Gürbüz, Gürkan

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The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance by Pehlivan, Davut, Bayram, Yavuz, Gunes, Nilay, Coban Akdemir, Zeynep, Shukla, Anju, Bierhals, Tatjana, Tabakci, Burcu, Sahin, Yavuz, Gezdirici, Alper, Fatih, Jawid M., Gulec, Elif Yilmaz, Yesil, Gozde, Punetha, Jaya, Ocak, Zeynep, Grochowski, Christopher M., Karaca, Ender, Albayrak, Hatice Mutlu, Radhakrishnan, Periyasamy, Erdem, Haktan Bagis, Sahin, Ibrahim, Yildirim, Timur, Bayhan, Ilhan A., Bursali, Aysegul, Elmas, Muhsin, Yuksel, Zafer, Ozdemir, Ozturk, Silan, Fatma, Yildiz, Onur, Yesilbas, Osman, Isikay, Sedat, Balta, Burhan, Gu, Shen, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Tsiakas, Konstantinos, Hempel, Maja, Girisha, Katta Mohan, Gul, Davut, Posey, Jennifer E., Elcioglu, Nursel H., Tuysuz, Beyhan, Lupski, James R.

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Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey by Kiral, Eylem, Kirel, Birgul, Havan, Merve, Keskin, Mehmet, Karaoglan, Murat, Yildirim, Ahmet, Kangin, Murat, Talay, Mehmet Nur, Urun, Tuba, Altug, Umit, Kesici, Selman, Tufan, Erennur, Kacmaz, Ebru, Bozan, Gurkan, Azapagasi, Ebru, Uysal Yazici, Mutlu, Ozturk, Zeynelabidin, Yesilbas, Osman, Karaguzel, Gulay, Kaya, Gulay, Barlas, Ulkem, Duyu, Muhterem, Boyraz, Merve, Sevketoglu, Esra, Akcay, Nihal, Hancili, Suna, Guven, Ayla, Dursun, Oǧuz, Ulgen Tekerek, Nazan, Ozcifci, Gokçen, Yazici, Pinar, Turanli, Eda, Kendirli, Tanil, Kahveci, Fevzi, Yetimakman, Ayse Filiz, Citak, Agop, Şik, Guntulu, Bingol, Ibrahim, Aygun, Fatih, Durak, Cansu, Yilmaz, Resul, Bugrul, Fuat, Sari, Yusuf, Tekguç, Hakan, Albayrak, Hatice, Yener, Nazik, Agin, Hasan, Soydan, Ekin, Yildizdas, Dincer, Dilek, Semine Ozdemir, Yalindag, Nilufer, Incekoy-Girgin, Feyza, Alacakir, Nuri, Tutunculer, Filiz, Arslanaoglu, Mehmet Ozgur, Aydin, Can, Bilgin, Muzaffer, Simsek, Enver, Dinleyici, Ener Cagri

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