Novel hybrid primers for sequencing of the mitochondrial cytochrome b gene in the rabbitfishes (Teleostei: Siganidae) von Kiper, I. E., Hoareau, T. B.

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A lower X-gate in TASK channels traps inhibitors within the vestibule von Rödström, Karin E. J., Kiper, Aytuğ K., Zhang, Wei, Rinné, Susanne, Pike, Ashley C. W., Goldstein, Matthias, Conrad, Linus J., Delbeck, Martina, Hahn, Michael G., Meier, Heinrich, Platzk, Magdalena, Quigley, Andrew, Speedman, David, Shrestha, Leela, Mukhopadhyay, Shubhashish M. M., Burgess-Brown, Nicola A., Tucker, Stephen J., Müller, Thomas, Decher, Niels, Carpenter, Elisabeth P.

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Diagnostic yield of microarrays in individuals with non‐syndromic developmental delay and intellectual disability von Oğuz, S., Arslan, U. E., Kiper, P. Ö. Ş., Alikaşifoğlu, M., Boduroğlu, K., Utine, G. E.

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Diagnostic yield of whole‐exome sequencing in non‐syndromic intellectual disability von Taşkıran, E. Z., Karaosmanoğlu, B., Koşukcu, C., Ürel‐Demir, G., Akgün‐Doğan, Ö., Şimşek‐Kiper, P. Ö., Alikaşifoğlu, M., Boduroğlu, K., Utine, G. E.

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More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome von Dhooge, Tibbe, Van Damme, Tim, Syx, Delfien, Mosquera, Laura M., Nampoothiri, Sheela, Radhakrishnan, Anil, Simsek‐Kiper, Pelin O., Utine, Gülen E., Bonduelle, Maryse, Migeotte, Isabelle, Essawi, Osama, Ceylaner, Serdar, Al Kindy, Adila, Tinkle, Brad, Symoens, Sofie, Malfait, Fransiska

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Kinetic magnetism in triangular moiré materials von Ciorciaro, L., Smoleński, T., Morera, I., Kiper, N., Hiestand, S., Kroner, M., Zhang, Y., Watanabe, K., Taniguchi, T., Demler, E., İmamoğlu, A.

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Clinical and molecular analysis of RASopathies in a group of Turkish patients von Şimşek-Kiper, PÖ, Alanay, Y, Gülhan, B, Lissewski, C, Türkyılmaz, D, Alehan, D, Çetin, M, Utine, GE, Zenker, M, Boduroğlu, K

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Genetic IGF1R defects: new cases expand the spectrum of clinical features von Gonc, E. N., Ozon, Z. A., Oguz, S., Kabacam, S., Taskiran, E. Z., Kiper, P. O. S., Utine, G. E., Alikasifoglu, A., Kandemir, N., Boduroglu, O. K., Alikasifoglu, M.

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RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome von Bögershausen, Nina, Tsai, I-Chun, Pohl, Esther, Kiper, Pelin Özlem Simsek, Beleggia, Filippo, Percin, E Ferda, Keupp, Katharina, Matchan, Angela, Milz, Esther, Alanay, Yasemin, Kayserili, Hülya, Liu, Yicheng, Banka, Siddharth, Kranz, Andrea, Zenker, Martin, Wieczorek, Dagmar, Elcioglu, Nursel, Prontera, Paolo, Lyonnet, Stanislas, Meitinger, Thomas, Stewart, A Francis, Donnai, Dian, Strom, Tim M, Boduroglu, Koray, Yigit, Gökhan, Li, Yun, Katsanis, Nicholas, Wollnik, Bernd

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Effects of Immersive Virtual Therapy as a Method Supporting Recovery of Depressive Symptoms in Post-Stroke Rehabilitation: Randomized Controlled Trial von Kiper, Pawel, Przysiezna, Ewa, Cieslik, Blazej, Broniec-Siekaniec, Katarzyna, Kucinska, Aleksandra, Szczygiel, Jaroslaw, Turek, Katarzyna, Gajda, Robert, Szczepanska-Gieracha, Joanna

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ADA2 deficiency in a patient with Noonan syndrome‐like disorder with loose anagen hair: The co‐occurrence of two rare syndromes von Akgun‐Dogan, Ozlem, Simsek‐Kiper, Pelin O., Taskiran, Ekim, Lissewski, Christina, Brinkmann, Julia, Schanze, Denny, Göçmen, Rahşan, Cagdas, Deniz, Bilginer, Yelda, Utine, Gülen E., Zenker, Martin, Ozen, Seza, Tezcan, İlhan, Alikasifoglu, Mehmet, Boduroğlu, Koray

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Typical Face, Developmental Delay, and Hearing Loss in a Patient with 3M Syndrome: The Co-Occurrence of Two Rare Conditions von Akalın, Akçahan, Şimşek-Kiper, Pelin Ö., Taşkıran, Ekim, Utine, Gülen E., Boduroğlu, Koray

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Dimensions of wisdom perception across twelve countries on five continents von Rudnev, M., Barrett, H. C., Buckwalter, W., Machery, E., Stich, S., Barr, K., Bencherifa, A., Clancy, R. F., Crone, D. L., Deguchi, Y., Fabiano, E., Fodeman, A. D., Guennoun, B., Halamová, J., Hashimoto, T., Homan, J., Kanovský, M., Karasawa, K., Kim, H., Kiper, J., Lee, M., Liu, X., Mitova, V., Nair, R. B., Pantovic, L., Porter, B., Quintanilla, P., Reijer, J., Romero, P. P., Singh, P., Tber, S., Wilkenfeld, D. A., Yi, L., Grossmann, I.

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An eight‐case 1q21 region series: novel aberrations and clinical variability with new features von Ceylan, A. C., Sahin, I., Erdem, H. B., Kayhan, G., Simsek‐Kiper, P. O., Utine, G. E., Percin, F., Boduroglu, K., Alikasifoglu, M.

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Clinical and Radiographic Features of the Autosomal Recessive form of Brachyolmia Caused by PAPSS2 Mutations von Iida, Aritoshi, Simsek-Kiper, Pelin Özlem, Mizumoto, Shuji, Hoshino, Touma, Elcioglu, Nursel, Horemuzova, Eva, Geiberger, Stefan, Yesil, Gozde, Kayserili, Hülya, Utine, Gülen Eda, Boduroglu, Koray, Watanabe, Shigehiko, Ohashi, Hirofumi, Alanay, Yasemin, Sugahara, Kazuyuki, Nishimura, Gen, Ikegawa, Shiro

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Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders von Batkovskyte, Dominyka, McKenzie, Fiona, Taylan, Fulya, Simsek‐Kiper, Pelin Ozlem, Nikkel, Sarah M, Ohashi, Hirofumi, Stevenson, Roger E, Ha, Thuong, Cavalcanti, Denise P, Miyahara, Hiroyuki, Skinner, Steven A, Aguirre, Miguel A, Akçören, Zühal, Utine, Gulen Eda, Chiu, Tillie, Shimizu, Kenji, Hammarsjö, Anna, Boduroglu, Koray, Moore, Hannah W, Louie, Raymond J, Arts, Peer, Merrihew, Allie N, Babic, Milena, Jackson, Matilda R, Papadogiannakis, Nikos, Lindstrand, Anna, Nordgren, Ann, Barnett, Christopher P, Scott, Hamish S, Chagin, Andrei S, Nishimura, Gen, Grigelioniene, Giedre

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Café noir spots: a feature of familial progressive hyper‐ and hypopigmentation von Gülseren, D., Güleray, N., Akgün‐Doğan, Ö., Şimşek‐Kiper, P.Ö., Utine, E.G., Alikaşifoğlu, M., Ersoy‐Evans, S.

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International management platform for children’s interstitial lung disease (chILD-EU) von Griese, Matthias, Seidl, Elias, Hengst, Meike, Reu, Simone, Rock, Hans, Anthony, Gisela, Kiper, Nural, Emiralioğlu, Nagehan, Snijders, Deborah, Goldbeck, Lutz, Leidl, Reiner, Ley-Zaporozhan, Julia, Krüger-Stollfuss, Ingrid, Kammer, Birgit, Wesselak, Traudl, Eismann, Claudia, Schams, Andrea, Neuner, Doerthe, MacLean, Morag, Nicholson, Andrew G, Lauren, McCann, Clement, Annick, Epaud, Ralph, de Blic, Jacques, Ashworth, Michael, Aurora, Paul, Calder, Alistair, Wetzke, Martin, Kappler, Matthias, Cunningham, Steve, Schwerk, Nicolaus, Bush, Andy

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Further delineation of spondyloepimetaphyseal dysplasia Faden‐Alkuraya type: A RSPRY1‐associated spondylo‐epi‐metaphyseal dysplasia with cono‐brachydactyly and craniosynostosis... von Simsek‐Kiper, Pelin O., Taskiran, Ekim Z., Kosukcu, Can, Urel‐Demir, Gizem, Akgun‐Dogan, Ozlem, Yilmaz, Guney, Utine, Gulen E., Nishimura, Gen, Boduroglu, Koray, Alikasifoglu, Mehmet

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A Novel Missense LIG4 Mutation in a Patient With a Phenotype Mimicking Behçet’s Disease von Taskiran, Ekim Z., Sonmez, Hafize E., Kosukcu, Can, Tavukcuoglu, Ece, Yazici, Gozde, Esendagli, Gunes, Batu, Ezgi D., Kiper, Pelin O. S., Bilginer, Yelda, Alikasifoglu, Mehmet, Ozen, Seza

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