Langerhans Cell Histiocytosis: Single Center Experience of 25 Years von Tuysuz, G, Yildiz, I, Ozdemir, N, Adaletli, I, Kurugoglu, S, Apak, H, Dervisoglu, S, Bozkurt, S, Celkan, T

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253 Management of Hemangiomas: A Single Center Experience von Tuysuz, G, Ozdemir, N, Kutlubay, B, Celkan, T

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746 Glazmann Thrombasthenia: Single Center Experience von Kutlubay, B, Ozdemir, N, Tuysuz, G, Apak, H, Celkan, T

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A randomized comparison of sequential and single step culture media systems on sibling oocytes: complete P-1 versus single step medium von Donmez, E, Sati, L, Tuysuz, G, Gokalp Kaya, D, Celik, S, Demirel, L.C

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PO-0163Effect Of Nutrition With Follow-up Formula From 6th Month Of Age On The Complete Blood Count And Iron Levels Of Infants (preliminary Trial) von Apak, H, Ozdemir, N, Tuysuz, G, Kutlubay, B, Erginoz, E, Kucur, M

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Effect of nutrition with follow-up formula from 6th month of age on the complete blood count and iron levels of infants (preliminary Trial) von Apak, H, Ozdemir, N, Tuysuz, G, Kutlubay, B, Erginoz, E, Kucur, M

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PO-0163 Effect Of Nutrition With Follow-up Formula From 6th Month Of Age On The Complete Blood Count And Iron Levels Of Infants (preliminary Trial) von Apak, H, Ozdemir, N, Tuysuz, G, Kutlubay, B, Erginoz, E, Kucur, M

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Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity von Bachmann-Gagescu, R, Dempsey, J C, Phelps, I G, O'Roak, B J, Knutzen, D M, Rue, T C, Ishak, G E, Isabella, C R, Gorden, N, Adkins, J, Boyle, E A, de Lacy, N, O'Day, D, Alswaid, A, Ramadevi A, Radha, Lingappa, L, Lourenço, C, Martorell, L, Garcia-Cazorla, À, Ozyürek, H, Haliloğlu, G, Tuysuz, B, Topçu, M, Chance, P, Parisi, M A, Glass, I A, Shendure, J, Doherty, D

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Modeling rotavirus infection and antiviral therapy using primary intestinal organoids von Yin, Yuebang, Bijvelds, Marcel, Dang, Wen, Xu, Lei, van der Eijk, Annemiek A., Knipping, Karen, Tuysuz, Nesrin, Dekkers, Johanna F., Wang, Yijin, de Jonge, Jeroen, Sprengers, Dave, van der Laan, Luc J.W., Beekman, Jeffrey M., ten Berge, Derk, Metselaar, Herold J., de Jonge, Hugo, Koopmans, Marion P.G., Peppelenbosch, Maikel P., Pan, Qiuwei

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XYLT1 Mutations in Desbuquois Dysplasia Type 2 von Bui, Catherine, Huber, Céline, Tuysuz, Beyhan, Alanay, Yasemin, Bole-Feysot, Christine, Leroy, Jules G., Mortier, Geert, Nitschke, Patrick, Munnich, Arnold, Cormier-Daire, Valérie

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Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans von Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschké, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stéphane, Szabó, Attila J., Tory, Kálmán, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hülya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie, Hildebrandt, Friedhelm

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Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients von Santen, Gijs W.E., Aten, Emmelien, Vulto-van Silfhout, Anneke T., Pottinger, Caroline, van Bon, Bregje W.M., van Minderhout, Ivonne J.H.M., Snowdowne, Ronelle, van der Lans, Christian A.C., Boogaard, Merel, Linssen, Margot M.L., Vijfhuizen, Linda, van der Wielen, Michiel J.R., Vollebregt, M.J. (Ellen), Breuning, Martijn H., Kriek, Marjolein, van Haeringen, Arie, den Dunnen, Johan T., Hoischen, Alexander, Clayton-Smith, Jill, de Vries, Bert B.A., Hennekam, Raoul C.M., van Belzen, Martine J., Almureikhi, Mariam, Baban, Anwar, Barbosa, Mafalda, Ben-Omran, Tawfeg, Berry, Katherine, Bigoni, Stefania, Boute, Odile, Brueton, Louise, van der Burgt, Ineke, Canham, Natalie, Chandler, Kate E., Chrzanowska, Krystyna, Collins, Amanda L., de Toni, Teresa, Dean, John, den Hollander, Nicolette S., Flore, Leigh Anne, Fryer, Alan, Gardham, Alice, Graham Jr, John M., Harrison, Victoria, Horn, Denise, Jongmans, Marjolijn C., Josifova, Dragana, Kant, Sarina G., Kapoor, Seema, Kingston, Helen, Kini, Usha, Kleefstra, Tjitske, Krajewska-Walasek, Małgorzata, Kramer, Nancy, Maas, Saskia M., Maciel, Patricia, Mancini, Grazia M.S., Maystadt, Isabelle, McKee, Shane, Milunsky, Jeff M., Nampoothiri, Sheela, Newbury-Ecob, Ruth, Nikkel, Sarah M., Parker, Michael J., Pérez-Jurado, Luis A., Robertson, Stephen P., Rooryck, Caroline, Shears, Debbie, Silengo, Margherita, Singh, Ankur, Smigiel, Robert, Soares, Gabriela, Splitt, Miranda, Stewart, Helen, Sweeney, Elizabeth, Tassabehji, May, Tuysuz, Beyhan, van Eerde, Albertien M., Vincent-Delorme, Catherine, Wilson, Louise C., Yesil, Gozde

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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery von Scott, Eric M, Halees, Anason, Itan, Yuval, Spencer, Emily G, He, Yupeng, Azab, Mostafa Abdellateef, Gabriel, Stacey B, Belkadi, Aziz, Boisson, Bertrand, Abel, Laurent, Clark, Andrew G, Alkuraya, Fowzan S, Casanova, Jean-Laurent, Gleeson, Joseph G

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Low-pressure-high-temperature metamorphism during extension in a Jurassic magmatic arc, Central Pontides, Turkey von Okay, A. I., Sunal, G., Tüysüz, O., Sherlock, S., Keskin, M., Kylander-Clark, A. R.C.

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Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome von Caglayan, Ahmet Okay, Tuysuz, Beyhan, Gül, Ece, Alkaya, Dilek Uludag, Yalcinkaya, Cengiz, Gleeson, Joseph G, Bilguvar, Kaya, Gunel, Murat

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IFT80 , which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy von Scambler, Peter J, Beales, Philip L, Bland, Elizabeth, Tobin, Jonathan L, Bacchelli, Chiara, Tuysuz, Beyhan, Hill, Josephine, Rix, Suzanne, Pearson, Chad G, Kai, Masatake, Hartley, Jane, Johnson, Colin, Irving, Melita, Elcioglu, Nursel, Winey, Mark, Tada, Masazumi

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An investigation on protection properties of Tantalum (V) oxide reinforced glass screens on unexposed breast tissue for mammography examinations von Alan, H.Y., ALMisned, G., Yilmaz, A., Susam, L.A., Ilik, E., Kilic, G., Ozturk, G., Tuysuz, B., Akkus, B., Tekin, H.O.

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THE NORTH ANATOLIAN FAULT: A NEW LOOK von Sengor, A M C, Tiiysiiz, Okan, Imren, Caner, Sakinc, Mehmet, Eyidogan, Haluk, Gorur, Naci, Le Pichon, Xavier, Rangin, Claude

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CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration von Schaffer, Ashleigh E., Eggens, Veerle R.C., Caglayan, Ahmet Okay, Reuter, Miriam S., Scott, Eric, Coufal, Nicole G., Silhavy, Jennifer L., Xue, Yuanchao, Kayserili, Hulya, Yasuno, Katsuhito, Rosti, Rasim Ozgur, Abdellateef, Mostafa, Caglar, Caner, Kasher, Paul R., Cazemier, J. Leonie, Weterman, Marian A., Cantagrel, Vincent, Cai, Na, Zweier, Christiane, Altunoglu, Umut, Satkin, N. Bilge, Aktar, Fesih, Tuysuz, Beyhan, Yalcinkaya, Cengiz, Caksen, Huseyin, Bilguvar, Kaya, Fu, Xiang-Dong, Trotta, Christopher R., Gabriel, Stacey, Reis, André, Gunel, Murat, Baas, Frank, Gleeson, Joseph G.

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Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum von Taylan, Fulya, Costantini, Alice, Coles, Nicole, Pekkinen, Minna, Héon, Elise, Şıklar, Zeynep, Berberoğlu, Merih, Kämpe, Anders, Kıykım, Ertuğrul, Grigelioniene, Giedre, Tüysüz, Beyhan, Mäkitie, Outi

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